AMUKINE 0.05% Topical solution

Зміст інструкції

1. Amukine Med 0.05% cutaneous spray, solution
   1. What is Amukine Med and what is it used for
   2. What you need to know before using Amukine Med
   3. How to use Amukine Med
   4. Possible side effects
   5. How to store Amukine Med
   6. Contents of the pack and other information
   7. CONTENTS
   8. EXPIRY DATE
   9. BATCH NUMBER
   10. MARKETING AUTHORISATION NUMBER(S)
   11. GENERAL CONDITIONS OF SUPPLY
   12. BRAILLE INFORMATION
   13. UNIQUE IDENTIFIER – TWO-DIMENSIONAL BARCODE
   14. UNIQUE IDENTIFIER - DATA MADE LEGIBLE
2. Amukine Med 0.05% cutaneous solution
   1. What is Amukine Med and what is it used for
   2. What you need to know before using Amukine Med
   3. How to use Amukine Med
   4. Possible side effects
   5. How to store Amukine Med
   6. Contents of the pack and other information
   7. CONTENT
   8. EXPIRY DATE
   9. BATCH NUMBER
   10. GENERAL SUPPLY CONDITION
   11. MARKETING AUTHORISATION NUMBER(S)
   12. BRAILLE INFORMATION
   13. UNIQUE IDENTIFIER – TWO-DIMENSIONAL BARCODE
   14. UNIQUE IDENTIFIER - READABLE DATA
3. Amukine Med 0.05% cutaneous solution
   1. What is Amukine Med and what is it used for
   2. What you need to know before using Amukine Med
   3. How to use Amukine Med
   4. Possible side effects
   5. How to store Amukine Med
   6. Contents of the pack and other information
   7. CONTENT
   8. EXPIRY DATE
   9. BATCH NUMBER
   10. GENERAL SUPPLY CONDITION
   11. MARKETING AUTHORISATION NUMBER(S)
   12. BRAILLE INFORMATION
   13. UNIQUE IDENTIFIER – TWO-DIMENSIONAL BARCODE
   14. UNIQUE IDENTIFIER - READABLE DATA
4. Amukine Med 0.05% cutaneous solution
   1. What is Amukine Med and what is it used for
   2. What you need to know before using Amukine Med
   3. How to use Amukine Med
   4. Possible side effects
   5. How to store Amukine Med
   6. Contents of the pack and other information
   7. CONTENT
   8. EXPIRY DATE
   9. BATCH NUMBER
   10. GENERAL CONDITIONS OF SUPPLY
   11. MARKETING AUTHORISATION NUMBER(S)
   12. BRAILLE INFORMATION
   13. UNIQUE IDENTIFIER – TWO-DIMENSIONAL BARCODE
   14. UNIQUE IDENTIFIER - DATA MADE LEGIBLE

Amukine Med 0.05% cutaneous spray, solution

Sodium hypochlorite

Read this leaflet carefully before using this medicine as it contains important
information for you.

• Use this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you.
• Keep this leaflet. You may need to read it again.
• If you want more information or advice, ask your pharmacist.
• If any side effects occur, including effects not listed in this leaflet, tell your doctor or pharmacist. See section 4.
• See a doctor if you do not feel better or if your symptoms worsen after a short period of treatment.

Contents of this leaflet:

• 1. What Amukine Med is and what it is used for
• 2. What you need to know before using Amukine Med
• 3. How to use Amukine Med
• 4. Possible side effects
• 5. How to store Amukine Med
• 6. Contents of the pack and other information

1. What is Amukine Med and what is it used for

Amukine Med contains sodium hypochlorite, an antiseptic for local use.
Amukine Med is indicated for:

• disinfecting and cleaning minor skin lesions such as superficial wounds of small size, pressure ulcers (skin lesions affecting parts of the body subjected to pressure for prolonged periods) of mild severity, burns (scalds) of mild severity (I degree);
• disinfecting the external genitalia.

Consult a doctor if you do not feel better or if you feel worse after a short period of treatment.

2. What you need to know before using Amukine Med

Do not useAmukine Med
If you are allergic to sodium hypochlorite or to any of the other ingredients of this medicine (listed in
section 6).

Warnings and precautions
Amukine Med is for external use only.
The use, especially if prolonged, of products for local use can give rise to allergic reactions (see
section “Possible side effects”). In this case, discontinue treatment and consult your doctor who
will establish the appropriate therapy.
The presence of organic materials (proteins, serum, blood, etc.) reduces the activity of the antiseptic.
Application of the product may dissolve blood clots and cause bleeding.
Avoid contact with eyes.

Other medicines and Amukine Med
Tell your doctor or pharmacist if you are taking, have recently taken or might take any
other medicines.
Avoid the simultaneous use of other antiseptics and detergents.

Pregnancy and breastfeeding
If you are pregnant, suspect you are pregnant or are planning a pregnancy, or if you are breastfeeding
with breast milk, ask your doctor or pharmacist for advice before using this medicine.
This medicine can be used during pregnancy and breastfeeding.

Driving and operating machinery
Not applicable.

3. How to use Amukine Med

Use this medicine following exactly as stated in this leaflet or as instructed by your doctor or pharmacist. If you have any doubts, consult your doctor or pharmacist.
Amukine Med 0.05% cutaneous spray is ready for use.
Apply the spray locally:

• directly onto the area to be treated (wounds, sores, burns),
• onto gauze pads,
• onto bandages. Dispense the spray until the area to be treated is evenly moistened. A single application is equivalent to 0.7 ml of solution.

Disinfection can be repeated if deemed necessary, but no more than 6 times a day.
Use this medicine only for short periods of treatment.

If you use more Amukine Med than you should
Accidental ingestion or inhalation may have serious consequences, which can even lead to death. In case of accidental ingestion of the product, consult a doctor immediately or go to the nearest hospital.

If you forget to use Amukine Med
Do not use a double dose to make up for a missed dose.

If you stop using Amukine Med
If you have any doubts about the use of this medicine, consult your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you experience an allergic reaction during treatment with Amukine Med STOPtreatment immediately
and consult your doctor.
The following side effects have been reported with the use of Amukine Med:

• intolerance (burning or irritation);
• redness and itching of the skin that has come into contact with the medicine (allergic contact dermatitis).

Reporting of side effects
If you experience any side effects, including those not listed in this leaflet, please inform your
doctor or pharmacist. You can also report side effects directly through the national reporting system at
https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse.
By reporting side effects you can help provide more information on the safety of
this medicine.

5. How to store Amukine Med

Keep this medicine out of the sight and reach of children.
Keep the bottle tightly closed to protect the medicine from light.
Replace the protective cap on the applicator after each use.
Do not use this medicine after 6 months from first opening.
This medicine does not require any particular storage temperature.
Do not use this medicine after the expiry date which is on the bottle after “Scad”. The expiry date refers to the last day of that month.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to dispose of
medicines you no longer use. This will help protect the environment.

6. Contents of the pack and other information

What Amukine Med contains
100 ml of solution contains
The active ingredient is sodium hypochlorite 0.057 g (active chlorine 0.055 g).
The other ingredients are: sodium chloride, sodium hydroxide, sodium bicarbonate, purified water.

Description of the appearance of Amukine Med and contents of the pack
Amukine Med 0.05% cutaneous spray solution is presented in the form of a solution for external use, which is
dispensed through a spray device.
The pack contains 200 ml.

Marketing authorisation holder and manufacturer
Angelini Pharma S.p.A.
Viale Amelia, 70 - 00181 Roma

Manufacturer
A.C.R.A.F. S.p.A. Via Pontasso, 13 – 16015 Casella (Genova)

A.C.R.A.F. S.p.A. Via Vecchia del Pinocchio, 22 60131 ANCONA
INFORMATION TO BE AFFIXED TO THE PRIMARY PACKAGING
BOTTLE

1. CONTENTS

Bottle of 200 ml

2. EXPIRY DATE

Exp

3. BATCH NUMBER

Batch

4. MARKETING AUTHORISATION NUMBER(S)

A.I.C. n. 032192041

5. GENERAL CONDITIONS OF SUPPLY

Over-the-counter medicine

6. BRAILLE INFORMATION

Amukine med 0,05% cutaneous spray, solution

17. UNIQUE IDENTIFIER – TWO-DIMENSIONAL BARCODE

Two-dimensional barcode with unique identifier included.

18. UNIQUE IDENTIFIER - DATA MADE LEGIBLE

PC:
SN:
NN:

Amukine Med 0.05% cutaneous solution

Sodium hypochlorite

Read this leaflet carefully before using this medicine as it contains important information for you.

• Always use this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you to.
• Keep this leaflet. You may need to read it again.
• If you want more information or advice, ask your pharmacist.
• If any side effects occur, including effects not listed in this leaflet, tell your doctor or pharmacist. See section 4.
• See a doctor if you do not feel better or if your symptoms worsen after a short period of treatment.

Contents of this leaflet:

• 1. What Amukine Med is and what it is used for
• 2. What you need to know before using Amukine Med
• 3. How to use Amukine Med
• 4. Possible side effects
• 5. How to store Amukine Med
• 6. Contents of the pack and other information

1. What is Amukine Med and what is it used for

Amukine Med contains sodium hypochlorite, an antiseptic for local use.
Amukine Med is indicated for:

• disinfecting and cleaning minor skin lesions such as small superficial wounds, pressure ulcers (skin lesions that affect parts of the body subjected to pressure for prolonged periods) of mild severity, minor burns (first degree);
• disinfecting the external genitalia.

Consult your doctor if you do not feel better or if you feel worse after a short period of treatment.

2. What you need to know before using Amukine Med

Do not useAmukine Med
If you are allergic to sodium hypochlorite or any of the other ingredients of this medicine (listed in
section 6).

Warnings and precautions
Amukine Med is for external use only.
The use, especially if prolonged, of products for local use may give rise to allergic reactions (see
section “Possible side effects”). In this case, discontinue treatment and consult your doctor who
will establish the appropriate therapy.
The presence of organic materials (proteins, serum, blood, etc.) may reduce the activity of the antiseptic.
Topical application of the product may dissolve blood clots and cause bleeding.
Avoid contact with eyes.

Other medicines and Amukine Med
Tell your doctor or pharmacist if you are taking, have recently taken or might take any
other medicines.
Avoid the simultaneous use of other antiseptics or detergents.

Pregnancy and breastfeeding
If you are pregnant, suspect or are planning a pregnancy, or if you are breastfeeding, ask your doctor or
pharmacist for advice before using this medicine.
This medicine can be used during pregnancy and breastfeeding.

Driving and operating machinery
Not applicable.

3. How to use Amukine Med

Use this medicine following exactly the instructions in this leaflet, or as directed by your doctor or pharmacist. If you have any doubts, ask your doctor or pharmacist.
Amukine Med 0.05% cutaneous solution is ready for use.
Apply the solution locally by means of:

• washing or bathing,
• soaked compresses,
• moistened dressings.

Disinfection can be repeated if deemed necessary, but no more than 6 times a day.
Use this medicine only for short periods of treatment.

If you use more Amukine Med than you should
Accidental ingestion or inhalation may have serious consequences, which may even lead to death. In case of accidental ingestion of the product, consult a doctor immediately, or go to the nearest hospital.

If you forget to use Amukine Med
Do not use a double dose to make up for a missed dose.

If you stop using Amukine Med
If you have any doubts about the use of this medicine, ask your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you experience an allergic reaction during treatment with Amukine Med, STOP treatment immediately
and consult your doctor.
The following side effects may occur with the use of Amukine Med:

• intolerance (burning or irritation);
• redness and itching of the skin that has come into contact with the medicine (allergic contact dermatitis).

Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. You can also report side effects directly
through the national reporting system at https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse
By reporting side effects you can help provide more information on the safety of
this medicine.

5. How to store Amukine Med

Keep this medicine out of the sight and reach of children.
Keep the bottle tightly closed to protect the medicine from light.
Do not use this medicine after 6 months from first opening.
This medicine does not require any particular storage temperature.
Do not use this medicine after the expiry date which is on the bottle after {SCAD}. The expiry date refers to
the last day of that month.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to eliminate
medicines that you no longer use. This will help protect the environment.

6. Contents of the pack and other information

What Amukine Med contains
100 ml of solution contains
The active ingredient is sodium hypochlorite 0.57 g (active chlorine 0.055 g).
The other ingredients are: sodium chloride, sodium hydroxide, sodium bicarbonate, purified water.

Description of the appearance of Amukine Med and contents of the pack
Amukine Med 0.05% cutaneous solution is presented in the form of a solution for external use.
The pack contains 250, 500 or 1000 ml.
Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer
Angelini Pharma S.p.A.
Viale Amelia, 70 - 00181 Rome

Manufacturer
A.C.R.A.F. S.p.A. Via Pontasso, 13 – 16015 Casella (Genoa)
A.C.R.A.F. S.p.A. Via Vecchia del Pinocchio, 22 60131 ANCONA

------------------------------------------------------------------------------------------------------------------------------
MINIMUM INFORMATION TO BE AFFIXED ON THE PRIMARY PACKAGING
BOTTLE

1. CONTENT

Bottle of 250 ml

2. EXPIRY DATE

Exp.

3. BATCH NUMBER

Batch no.

4. GENERAL SUPPLY CONDITION

Over-the-counter medicine

5. MARKETING AUTHORISATION NUMBER(S)

AIC n.032192015

6. BRAILLE INFORMATION

Amukine Med 0.05% cutaneous solution

17. UNIQUE IDENTIFIER – TWO-DIMENSIONAL BARCODE

Two-dimensional barcode with a unique identifier included.

18. UNIQUE IDENTIFIER - READABLE DATA

PC:
SN:
NN:

Amukine Med 0.05% cutaneous solution

Sodium hypochlorite

Read this leaflet carefully before using this medicine as it contains important information for you.

• Always use this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you to.
• Keep this leaflet. You may need to read it again.
• If you want more information or advice, ask your pharmacist.
• If any side effects occur, including effects not listed in this leaflet, tell your doctor or pharmacist. See section 4.
• See a doctor if you do not feel better or if your symptoms worsen after a short period of treatment.

Contents of this leaflet:

• 1. What Amukine Med is and what it is used for
• 2. What you need to know before using Amukine Med
• 3. How to use Amukine Med
• 4. Possible side effects
• 5. How to store Amukine Med
• 6. Contents of the pack and other information

1. What is Amukine Med and what is it used for

Amukine Med contains sodium hypochlorite, an antiseptic for local use.
Amukine Med is indicated for:

• disinfecting and cleaning minor skin lesions such as small superficial wounds, pressure ulcers (skin lesions that affect parts of the body subjected to pressure for prolonged periods) of mild severity, minor burns (first degree);
• disinfecting the external genitalia.

Consult your doctor if you do not feel better or if you feel worse after a short period of treatment.

2. What you need to know before using Amukine Med

Do not useAmukine Med
If you are allergic to sodium hypochlorite or any of the other ingredients of this medicine (listed in
section 6).

Warnings and precautions
Amukine Med is for external use only.
The use, especially if prolonged, of products for local use can give rise to allergic reactions (see
section “Possible undesirable effects”). In this case, discontinue treatment and consult your doctor who
will establish the appropriate therapy.
The presence of organic materials (proteins, serum, blood, etc.) may reduce the activity of the antiseptic.
Topical application of the product may dissolve blood clots and cause bleeding.
Avoid contact with eyes.

Other medicines and Amukine Med
Tell your doctor or pharmacist if you are taking, have recently taken or might take any
other medicines.
Avoid the simultaneous use of other antiseptics or detergents.

Pregnancy and breastfeeding
If you are pregnant, suspect you are pregnant or are planning a pregnancy, or if you are breastfeeding,
ask your doctor or pharmacist for advice before using this medicine.
This medicine can be used during pregnancy and breastfeeding.

Driving and operating machinery
Not applicable.

3. How to use Amukine Med

Use this medicine following exactly as stated in this leaflet or as instructed by your doctor or pharmacist. If you have any doubts, consult your doctor or pharmacist.
Amukine Med 0.05% cutaneous solution is ready for use.
Apply the solution locally by means of:

• Washing or bathing,
• soaked compresses,
• moistened dressings.

Disinfection may be repeated if deemed necessary, but no more than 6 times a day.
Use this medicine only for short periods of treatment.

If you use more Amukine Med than you should
Accidental ingestion or inhalation may have serious consequences, which can even lead to death. In case of accidental ingestion of the product, consult a doctor immediately, or go to the nearest hospital.

If you forget to use Amukine Med
Do not use a double dose to make up for a missed dose.

If you stop using Amukine Med
If you have any doubts about the use of this medicine, consult your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you experience an allergic reaction during treatment with Amukine Med, STOP treatment immediately
and consult your doctor.
The following side effects may occur with the use of Amukine Med:

• intolerance (burning or irritation);
• redness and itching of the skin that comes into contact with the medicine (allergic contact dermatitis).

Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. You can also report side effects directly
through the national reporting system at https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse.
By reporting side effects you can help provide more information on the safety of
this medicine.

5. How to store Amukine Med

Keep this medicine out of the sight and reach of children.
Keep the bottle tightly closed to protect the medicine from light.
Do not use this medicine after 6 months from first opening.
This medicine does not require any particular storage temperature.
Do not use this medicine after the expiry date which is on the bottle after {SCAD}. The expiry date refers to
the last day of that month.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to eliminate
medicines that you no longer use. This will help protect the environment.

6. Contents of the pack and other information

What Amukine Med contains
100 ml of solution contains
The active ingredient is sodium hypochlorite 0.57 g (active chlorine 0.055 g).
The other ingredients are: sodium chloride, sodium hydroxide, sodium bicarbonate, purified water.

Description of the appearance of Amukine Med and contents of the pack
Amukine Med 0.05% cutaneous solution is presented in the form of a solution for external use.
The pack contains 250, 500 or 1000 ml.
Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer
Angelini Pharma S.p.A.
Viale Amelia, 70 - 00181 Rome

Manufacturer
A.C.R.A.F. S.p.A. Via Pontasso, 13 – 16015 Casella (Genoa)
A.C.R.A.F. S.p.A. Via Vecchia del Pinocchio, 22 60131 ANCONA

------------------------------------------------------------------------------------------------------------------------------
MINIMUM INFORMATION TO BE STATED ON PRIMARY PACKAGING
BOTTLE

1. CONTENT

500 ml bottle

2. EXPIRY DATE

Exp.

3. BATCH NUMBER

Batch no.

4. GENERAL SUPPLY CONDITION

Over-the-counter medicine

5. MARKETING AUTHORISATION NUMBER(S)

AIC n.032192027

6. BRAILLE INFORMATION

Amukine Med 0.05% cutaneous solution

17. UNIQUE IDENTIFIER – TWO-DIMENSIONAL BARCODE

Two-dimensional barcode with unique identifier included.

18. UNIQUE IDENTIFIER - READABLE DATA

PC:
SN:
NN:

Amukine Med 0.05% cutaneous solution

Sodium hypochlorite

Read this leaflet carefully before using this medicine as it contains important
information for you.

• Always use this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you to do.
• Keep this leaflet. You may need to read it again.
• If you want more information or advice, ask your pharmacist.
• If any side effects occur, including effects not listed in this leaflet, tell your doctor or pharmacist. See section 4.
• See a doctor if you do not feel better or if your symptoms worsen after a short period of treatment.

Contents of this leaflet:

• 1. What Amukine Med is and what it is used for
• 2. What you need to know before you use Amukine Med
• 3. How to use Amukine Med
• 4. Possible side effects
• 5. How to store Amukine Med
• 6. Contents of the pack and other information

1. What is Amukine Med and what is it used for

Amukine Med contains sodium hypochlorite, an antiseptic for local use.
Amukine Med is indicated for:

• disinfecting and cleaning minor skin lesions such as superficial wounds of small size, pressure ulcers (skin lesions that affect parts of the body subjected to pressure for prolonged periods) of mild severity, minor burns (I degree);
• disinfecting the external genitalia.

Consult your doctor if you do not feel better or if you feel worse after a short period of treatment.

2. What you need to know before using Amukine Med

Do not useAmukine Med
If you are allergic to sodium hypochlorite or to any of the other ingredients of this medicine (listed in
section 6).

Warnings and precautions
Amukine Med is for external use only.
The use, especially if prolonged, of products for local use can give rise to allergic reactions (see
section “Possible side effects”). In this case, discontinue treatment and consult your doctor who
will establish the appropriate therapy.
The presence of organic materials (proteins, serum, blood, etc.) may reduce the activity of the antiseptic.
Topical application of the product may dissolve blood clots and cause bleeding.
Avoid contact with eyes.

Other medicines and Amukine Med
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any
other medicines.
Avoid the simultaneous use of other antiseptics or detergents.

Pregnancy and breastfeeding
If you are pregnant, suspect you are pregnant, or are planning a pregnancy, or if you are breastfeeding,
ask your doctor or pharmacist for advice before using this medicine.
This medicine can be used during pregnancy and breastfeeding.

Driving and operating machinery
Not applicable.

3. How to use Amukine Med

Use this medicine following exactly as stated in this leaflet, or as instructed by your doctor or pharmacist. If you have any doubts, consult your doctor or pharmacist.
Amukine Med 0.05% cutaneous solution is ready for use.
Apply the solution locally by means of:

• Washing or bath,
• soaked compresses,
• moist dressings.

Disinfection can be repeated if deemed necessary, but no more than 6 times a day.
Use this medicine only for short periods of treatment.

If you use more Amukine Med than you should
Accidental ingestion or inhalation may have serious consequences, which may even lead to death. In case of accidental ingestion of the product, consult a doctor immediately, or go to the nearest
hospital.

If you forget to use Amukine Med
Do not use a double dose to make up for a missed dose.

If you stop using Amukine Med
If you have any doubts about the use of this medicine, consult your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you experience an allergic reaction during treatment with Amukine Med, STOP treatment immediately
and consult your doctor.
The following side effects may occur with the use of Amukine Med:

• intolerance (burning or irritation);
• redness and itching of the skin that comes into contact with the medicine (allergic contact dermatitis).

Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. You can also report side effects directly
through the national reporting system at https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse.
By reporting side effects you can help provide more information on the safety of
this medicine.

5. How to store Amukine Med

Keep this medicine out of the sight and reach of children.
Keep the bottle tightly closed to protect the medicine from light.
Do not use this medicine after 6 months from first opening.
This medicine does not require any particular storage temperature.
Do not use this medicine after the expiry date which is on the bottle after {SCAD}. The expiry date refers to
the last day of that month.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to eliminate
medicines that you no longer use. This will help protect the environment.

6. Contents of the pack and other information

What Amukine Med contains
100 ml of solution contains
The active ingredient is sodium hypochlorite 0.57 g (active chlorine 0.055 g).
The other ingredients are: sodium chloride, sodium hydroxide, sodium bicarbonate, purified water.

Description of the appearance of Amukine Med and contents of the pack
Amukine Med 0.05% cutaneous solution is presented in the form of a solution for external use.
The pack contains 250, 500 or 1000 ml.
Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer
Angelini Pharma S.p.A.
Viale Amelia, 70 - 00181 Rome

Manufacturer
A.C.R.A.F. S.p.A. Via Pontasso, 13 – 16015 Casella (Genoa)
A.C.R.A.F. S.p.A. Via Vecchia del Pinocchio, 22 60131 ANCONA

------------------------------------------------------------------------------------------------------------------------------
MINIMUM INFORMATION TO BE STATED ON PRIMARY PACKAGING
FLACON

1. CONTENT

Bottle of 1000 ml

2. EXPIRY DATE

Exp.

3. BATCH NUMBER

Batch no.

4. GENERAL CONDITIONS OF SUPPLY

Over-the-counter medicine

5. MARKETING AUTHORISATION NUMBER(S)

AIC n.032192039

6. BRAILLE INFORMATION

Amukine Med 0.05% cutaneous solution

17. UNIQUE IDENTIFIER – TWO-DIMENSIONAL BARCODE

Two-dimensional barcode with a unique identifier included.

18. UNIQUE IDENTIFIER - DATA MADE LEGIBLE

PC:
SN:
NN: