Label: DANDRUFF- pyrithione zinc 1% shampoo
- NDC Code(s): 41250-281-15, 41250-281-32, 41250-281-35
- Packager: Meijer Distribution, Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 25, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Claims
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
-
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, Prunus amygdalus dulcis (sweet almond) oil, methylchloroisothiazolinone, methylisothiazolinone
- Disclaimer
- Adverse Reactions
- Principal display panel
-
INGREDIENTS AND APPEARANCE
DANDRUFF
pyrithione zinc 1% shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-281 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) ALMOND OIL (UNII: 66YXD4DKO9) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-281-15 420 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/24/2002 2 NDC:41250-281-35 700 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/24/2002 3 NDC:41250-281-32 370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 05/24/2002 Labeler - Meijer Distribution, Inc (006959555) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(41250-281) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(41250-281)