Label: 2 IN 1 DANDRUFF- pyrithione zinc shampoo
- NDC Code(s): 55910-311-15, 55910-311-32, 55910-311-35, 55910-311-86
- Packager: OLD EAST MAIN CO.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 19, 2024
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Inactive ingredients
water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, sodium xylenesulfonate, amodimethicone, cocamidopropyl betaine, fragrance, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, citric acid, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33
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INGREDIENTS AND APPEARANCE
2 IN 1 DANDRUFF
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-311 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM CHLORIDE (UNII: 451W47IQ8X) ZINC CARBONATE (UNII: EQR32Y7H0M) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) AMODIMETHICONE (800 CST) (UNII: 363Z2T48P7) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM BENZOATE (UNII: OJ245FE5EU) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-311-15 420 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/23/2005 2 NDC:55910-311-32 369.7 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/23/2005 3 NDC:55910-311-35 700 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/23/2005 12/18/2022 4 NDC:55910-311-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/23/2005 05/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 06/23/2005 Labeler - OLD EAST MAIN CO. (068331990) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(55910-311) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(55910-311)