Label: HEAD REMEDY DANDRUFF CONDITIONER- pyrithione zinc emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 25237-0516-1 - Packager: KPSS, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 19, 2010
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INACTIVE INGREDIENT
water, cetearyl alcohol, isopropyl palmitate, stearamidopropyl dimethylamine, phenethyl dimethicone, mineral oil, lactic acid, panthenol, butylene glycol, propylene glycol, glucose, Foeniculum vulgare (Fennel) fruit extract, Melissa officinalis (Balm) extract, Salvia officinalis (Sage) extract, Rosmarinus officinalis (Rosemary) extract, Urtica dioica (Nettle) extract, Equisetum arvense (Horsetail) extract, Humulus lupulus (Hops) extract, Chamomilla recutita (Matricaria) flower extract, caramel, sorbitol, sodium benzoate, potassium sorbate, DMDM Hydantoin, phenoxyethanol, tartaric acid, methylparaben, propylparaben, isobutylparaben, ethylparaben, butylparaben, fragrance, blue 1
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INGREDIENTS AND APPEARANCE
HEAD REMEDY DANDRUFF CONDITIONER
pyrithione zinc emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:25237-0516 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1.0 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:25237-0516-1 249.4 g in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 01/01/2006 Labeler - KPSS, Inc. (808543149)