Pouxit Flash Shampooing 3 en 1

Organization name

Meda Pharma S.p.A.

SRN

IT-MF-000012233

Manufacturer status

Active

3 warnings recorded — scroll inside the panel to see all entries.

• CW007

  Do not use if packaging has been damaged before use.
• CW999

  Do not apply to irritated or damaged skin. Adults can carry out the treatment on their own, however getting help during application and combing can help to optimize results. The use in children should be carried out by an adult. If several family members are infested with head lice, treat all infested members with Linicin Shampoo 3in1 on the same day to avoid re-infestation. Use the included lice comb to check the hair of other family members for lice. Linicin Shampoo 3in1 is suitable for both adults and children from the age of 4 years old. There are no known risks in using Linicin Shampoo 3in1 during pregnancy and breast-feeding; it is however recommended to consult a physician or pharmacist before use. If Linicin Shampoo 3in1 is spilt on the floor or other surfaces they may become slippery. FOR EXTERNAL USE ONLY, DO NOT INGEST. IN CASE OF INGESTION, CONTACT A DOCTOR OR A POISON CONTROL CENTER, KEEP THE PACKAGE HANDY TO HELP THE DOCTOR TO IDENTIFY THE PRODUCT. Do not use Linicin Shampoo 3in1 after expiry date indicated on the carton box. After use, dispose the product according to current regulations on disposal of urban waste. Keep out of the sight and reach of children.
• CW999

  Linicin Shampoo 3in1 must not be used on/or by persons who are sensitive to any of the ingredients. If you are uncertain, try Linicin Shampoo 3in1 on a small skin area prior to first use. Discontinue use and consult your doctor should you experience a sensitive or allergic reaction or any other undesirable side effect. Avoid contact with eyes. If contact occurs, rinse well with water.

Primary placement in France; available across 1 country total.

Trade name

Pouxit Flash Shampooing 3 en 1

UDI-DI code

08058302780627

Basic UDI-DI

805830278LinicinShampooLD

Reference / catalog number

N.A.

Issuing entity

GS1

Risk category

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

European Medical Device Nomenclature — the EU product classification assigned to this device.

• V901001LICE ELIMINATION MECHANICAL DEVICES

Certificate health across this manufacturer's portfolio.