Label: HEAD AND SHOULDERS COCONUT DAILY HAIR AND SCALP CONDITIONER- pyrithione zinc lotion
- NDC Code(s): 69423-319-25, 69423-319-32
- 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 April 4, 2023
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Inactive ingredients
Water, stearyl alcohol, cetyl alcohol, stearamidopropyl dimethylamine, glutamic acid, dimethicone, fragrance, phenoxyethanol, benzyl alcohol, citric acid, sodium chloride, zea mays (corn) silk extract, orchis mascula flower extract, cocos nucifera (coconut) fruit extract, methylchloroisothiazolinone, methylisothiazolinone.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 325 mL Tube Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS COCONUT DAILY HAIR AND SCALP CONDITIONER
pyrithione zinc lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-319 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength COCONUT (UNII: 3RT3536DHY) WATER (UNII: 059QF0KO0R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CETYL ALCOHOL (UNII: 936JST6JCN) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) GLUTAMIC ACID (UNII: 3KX376GY7L) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) BENZYL ALCOHOL (UNII: LKG8494WBH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM CHLORIDE (UNII: 451W47IQ8X) CORN SILK (UNII: 7D3VB244UX) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) ORCHIS MASCULA FLOWER (UNII: 6H1JQK35LA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-319-32 325 mL in 1 TUBE; Type 0: Not a Combination Product 11/29/2018 2 NDC:69423-319-25 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/04/2018 01/02/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M032 11/29/2018 Labeler - The Procter & Gamble Manufacturing Company (004238200)