Label: HEAD AND SHOULDERS CLINICAL MOISTURIZING SCALP- pyrithione zinc cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69423-528-12 - Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 December 17, 2020
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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- Inactive ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 125 mL bottle
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS CLINICAL MOISTURIZING SCALP
pyrithione zinc creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-528 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 0.2 g in 100 mL Inactive Ingredients Ingredient Name Strength HONEY (UNII: Y9H1V576FH) GLUTAMIC ACID (UNII: 3KX376GY7L) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) BENZYL ALCOHOL (UNII: LKG8494WBH) CETYL ALCOHOL (UNII: 936JST6JCN) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLPARABEN (UNII: Z8IX2SC1OH) METHYLPARABEN (UNII: A2I8C7HI9T) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-528-12 125 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 11/17/2020 Labeler - The Procter & Gamble Manufacturing Company (004238200)