Active Ingredient
Pyrithione Zinc 1%
Equate Dry Scalp Dandruff
FDA Label NDC 49035-086
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 Equate Dry Scalp Dandruff (NDC 49035-086). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-dandruff
Uses
to help prevent reccurence of flaking and itching associated with dandruff
Warnings
For external use only.
When Using This Product
avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
condition worsens or does not improve after regular use of this product as directed
Keep Out Of Reach Of Children.
In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Directions
- for best results, use at least twice a week or as directed by a doctor.
- wet hair, massage onto scalp and rinse.
- repeat if desired.
Inactive Ingredients
Water (Aqua), Sodium Laureth Sulfate, Acrylates Copolymer, Cocamidopropyl Betaine, Prunus Amygdalus (Sweet Almond) Oil, Sodium Chloride, Glycol Distearate, Laureth-4, Sodium Hydroxide, Polyquaternium-113, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone.
Questions?
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Label Copy
Image Of The Label (22668l)
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