![CVS PHARMACY DANDRUFF (PYRITHIONE ZINC) LIQUID [CVS PHARMACY]](https://medic.hrt.org//dailymed/images/e45104ba-a3fd-496c-ae2d-4ec296eb6334/19172L.jpg)
- ACTIVE INGREDIENT
- USES
- WARNINGS
- DIRECTIONS
- QUESTIONS/COMMENTS?
-
INACTIVE INGREDIENTS
WATER (AQUA), AMMONIUM LAURETH SULFATE, AMMONIUM LAURYL SULFATE, GLYCERIN, GLYCOL DISTEARATE, COCAMIDE MEA, CETYL ALCOHOL, FRAGRANCE (PARFUM), ALOE BARBADENSIS LEAF JUICE, DIMETHICONE, TOCOPHERYL ACETATE, PANTHENOL, ACETAMIDOPROPYL TRIMONIUM CHLORIDE, LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE, PEG-3 DIOLEOYLAMIDOETHYLMONIUM METHOSULFATE, DIMETHICONOL, SODIUM LAURYL GLUCOSE CARBOXYLATE, LAURYL GLUCOSIDE, AMODIMETHICONE, HYDROXYPROPYL METHYLCELLULOSE, SODIUM DODECYLBENZENESULFONATE, LAURETH-9, DMDM HYDANTOIN, C11-15 PARETH-7, TRIDECETH-12, PROPYLENE GLYCOL, SODIUM CHLORIDE, CITRIC ACID, HYDROXYETHYLCELLULOSE, BLUE 1 (CI 42090)
- LABEL COPY
-
INGREDIENTS AND APPEARANCE
CVS PHARMACY DANDRUFF
pyrithione zinc liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-428 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) AMMONIUM LAURETH-3 SULFATE (UNII: 896SJ235FN) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) GLYCERIN (UNII: PDC6A3C0OX) GLYCOL DISTEARATE (UNII: 13W7MDN21W) COCO MONOETHANOLAMIDE (UNII: C80684146D) CETYL ALCOHOL (UNII: 936JST6JCN) ALOE VERA LEAF (UNII: ZY81Z83H0X) DIMETHICONE (UNII: 92RU3N3Y1O) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTHENOL (UNII: WV9CM0O67Z) ACETAMIDOPROPYL TRIMONIUM CHLORIDE (UNII: 2SQT0WU9CO) LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO) PEG-3 DISTEAROYLAMIDOETHYLMONIUM METHOSULFATE (UNII: 395MHJ5PUR) DIMETHICONOL (100000 CST) (UNII: OSA9UP217S) SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) AMODIMETHICONE (3500 CST) (UNII: 42AFE8JAOY) HYPROMELLOSES (UNII: 3NXW29V3WO) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) LAURETH-9 (UNII: 0AWH8BFG9A) DMDM HYDANTOIN (UNII: BYR0546TOW) C11-15 PARETH-7 (UNII: 261HPE0IS3) TRIDECETH-12 (UNII: YFY3KG5Y7O) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CHLORIDE (UNII: 451W47IQ8X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-428-11 325 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 12/05/2013 Labeler - CVS PHARMACY (062312574) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(59779-428)
