Label: BEVEL DANDRUFF SHAM AND CONDITIONER WITH HEMP SEED OIL- pyrithione zinc shampoo
- NDC Code(s): 69423-601-35
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 9, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Inactive ingredients
Water, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Glycol Distearate, Sodium Chloride, Zinc Carbonate, Dimethicone, Cocamidopropyl Betaine, Sodium Xylenesulfonate, Fragrance, Sodium Benzoate, Guar Hydroxypropyltrimonium Chloride, Magnesium Carbonate Hydroxide, Histidine, Cannabis Sativa Seed Oil, Methylchloroisothiazolinone, Methylisothiazolinone
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label
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INGREDIENTS AND APPEARANCE
BEVEL DANDRUFF SHAM AND CONDITIONER WITH HEMP SEED OIL
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-601 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 g in 100 mL Inactive Ingredients Ingredient Name Strength POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS) MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) SODIUM BENZOATE (UNII: OJ245FE5EU) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) COCONUT OIL (UNII: Q9L0O73W7L) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) WATER (UNII: 059QF0KO0R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CETYL ALCOHOL (UNII: 936JST6JCN) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) COCO MONOETHANOLAMIDE (UNII: C80684146D) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) ZINC CARBONATE (UNII: EQR32Y7H0M) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM CHLORIDE (UNII: 451W47IQ8X) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-601-35 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2022 06/29/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 03/01/2022 06/29/2024 Labeler - The Procter & Gamble Manufacturing Company (004238200) Establishment Name Address ID/FEI Business Operations The Procter & Gamble Manufacturing Company 005279245 manufacture(69423-601) , pack(69423-601)