Otc - Active Ingredient
Pyrithione Zinc
Walmart
FDA Label NDC 79903-899
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wal-mart Stores, Inc for the product Walmart (NDC 79903-899). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
For the relief of itching, redness and flaking associated with dandruff
Warnings
For External use
Otc - When Using
avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if condition worsens or does not improve after regular use of this product.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.
Dosage & Administration
- Adults and children 2 years and older.
- Shake well.
- Apply evenly to scalp. leave on for several minutes and then rinse off.
- Use at least twice per week or as directed by a doctor or pharmacist.
Inactive Ingredient
Water, Stearyl Alcohol, Behentrimonium Chloride, Cetyl Alcohol, Cocos Nucifera (Coconut) Oil,
Dimethicone, Fragrance, PPG-3 Benzyl Ether Ethylhexanoate, Lauryl PEG/PPG-18/18 Methicone,
Hydroxyethylcellulose, Sodium Hydroxide, Citric Acid, Methylchloroisothiazolinone,
Methylisothiazolinone.
Storage And Handling
Store at room temperature
Indications & Usage
Relieves itching , redness and flakes associated with Dandruff.
Package Label.Principal Display Panel
700 mL (06 22271 72)
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