Active Ingredient
Pyrithione Zinc 1%
P.o.v. 2 In 1 Dry Scalp Dandruff
FDA Label NDC 63148-410
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Apollo Health And Beauty Care Inc. for the product P.o.v. 2 In 1 Dry Scalp Dandruff (NDC 63148-410). 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 recurrence of flaking and itching associated with dandruff.
Warnings
For external use only.
When Using This Product
avoid contact with eyes. If contact occurs, rinse 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
Wet hair and apply evenly to scalp, massaging gently. Rinse thoroughly. Repeat as needed. For best results, use at least twice a week or as directed by a doctor.
Inactive Ingredients
Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Glycol Distearate, Cocamidopropyl Betaine, Acrylates Copolymer, Laureth-4, Fragrance (Parfum), Dimethicone, Cocamide MEA, Guar Hydroxypropyltrimonium Chloride, Sodium Hydroxide, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone.
Questions Or Comments?
1-866-695-3030
Label Copy
Image Of The Label (22803l)
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