Label: ANTI DANDRUFF SHAMPOOS- pyrithione zinc liquid
- NDC Code(s): 85434-002-01
- Packager: Guangdong Quaker Daily Chemical Co., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 26, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
-
INACTIVE INGREDIENT
water
sodium laureth sulfate
cocamidopropyl betaine
guar hydroxypropyltrimonium chloride
acrylates/c10-30 alkyl acrylate crosspolymer
zinc chloride
sodium chloride
methylchloroisothiazolinone
dimethicone
trideceth-3
trideceth-10
citric acid
prunus persica (peach) leaf extract
trehalose
aloe barbadensis leaf juice
ammonium lauryl sulfate
sodium benzoate
fragrance - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ANTI DANDRUFF SHAMPOOS
pyrithione zinc liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85434-002 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 COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) FRAGRANCE 13576 (UNII: 5EM498GW35) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) PRUNUS PERSICA LEAF (UNII: VN3501T41P) TREHALOSE (UNII: B8WCK70T7I) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) SODIUM BENZOATE (UNII: OJ245FE5EU) ALOE BARBADENSIS LEAF POWDER (UNII: ZY81Z83H0X) SODIUM CHLORIDE (UNII: 451W47IQ8X) TRIDECETH-10 (UNII: G624N6MSBA) CITRIC ACID (UNII: 2968PHW8QP) TRIDECETH-3 (UNII: 438A02204X) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) ZINC CHLORIDE (UNII: 86Q357L16B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85434-002-01 1 in 1 BOX 03/26/2025 1 473 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 03/26/2025 Labeler - Guangdong Quaker Daily Chemical Co., LTD (548075342) Establishment Name Address ID/FEI Business Operations Guangdong Quaker Daily Chemical Co., LTD 548075342 manufacture(85434-002)

