CVS PHARMACY DANDRUFF- pyrithione zinc liquid 
CVS PHARMACY

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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DRUG FACTS

ACTIVE INGREDIENT

PYRITHIONE ZINC 1%

PURPOSE

ANTIDANDRUFF

USES

TO HELP PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER

STOP USE AND ASK A DOCTOR IF

CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY

DIRECTIONS

SHAKE WELL. FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO. WET HAIR, MASSAGE ONTO SCALP AND RINSE. REPEAT IF DESIRED

QUESTIONS/COMMENTS?

1-800-746-7287

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

IMAGE OF THE LABEL

CVS PHARMACY  DANDRUFF
pyrithione zinc liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-428
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-428-11325 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H12/05/2013
Labeler - CVS PHARMACY (062312574)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(59779-428)

Revised: 12/2013
Document Id: 53863b72-f93a-4076-816a-f0b411b0ca88
Set id: e45104ba-a3fd-496c-ae2d-4ec296eb6334
Version: 1
Effective Time: 20131206
 
CVS PHARMACY