CVS PHARMACY COCONUT WATER- benzalkonium chloride 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.

----------

DRUG FACTS

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE 0.13%

PURPOSE

ANTIBACTERIAL

USES

FOR WASHING TO DECREASE BACTERIA ON THE SKIN

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

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

STOP USE AND ASK A DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

APPLY ONTO DRY HANDS. WORK INTO A LATHER, RINSE AND DRY THOROUGHLY

OTHER INFORMATION

STORE AT ROOM TEMPERATURE

INACTIVE INGREDIENTS

ALOE BARBADENSIS LEAF JUICE, BAMBUSA VULGARIS LEAF EXTRACT, BLUE 1 (CI 42090), CITRIC ACID, COCAMIDOPROPYL BETAINE, COCOS NUCIFERA (COCONUT) EXTRACT, DECYL GLUCOSIDE, FRAGRANCE (PARFUM), GLYCERIN, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, POLYQUATERNIUM-7, POLYSORBATE 20, RED 33 (CI 17200), SODIUM CITRATE, TETRASODIUM EDTA, WATER (AQUA), XANTHAN GUM

QUESTIONS OR COMMENTS?

1-800-746-7287

LABEL COPY

IMAGE OF THE LABEL

CVS PHARMACY  COCONUT WATER
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-842
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BAMBUSA VULGARIS LEAF (UNII: EMY54R518C)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
COCONUT OIL (UNII: Q9L0O73W7L)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-842-32946 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/26/2014
Labeler - CVS PHARMACY (062312574)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(59779-842)

Revised: 1/2014
Document Id: 36a44418-1c8d-4b42-a176-2b374fdc9000
Set id: 65684c92-e73a-41b4-9b3d-c0975d8266cf
Version: 1
Effective Time: 20140127
 
CVS PHARMACY