CVS PHARMACY CITRUS FRESH- 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.

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DRUG FACTS

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE 0.13%

PURPOSE

ANTIBACTERIAL

USES

HELPS ELIMINATE BACTERIA ON HANDS

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

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

STOP USING THIS PRODUCT 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 WET HANDS. LATHER AND RINSE THOROUGHLY

OTHER INFORMATION

STORE AT ROOM TEMPERATURE

INACTIVE INGREDIENTS

BLUE 1 (CI 42090), CAMELLIA SINENSIS LEAF EXTRACT, CETRIMONIUM CHLORIDE, CITRIC ACID, CITRUS NOBILIS (MANDARIN ORANGE) PEEL EXTRACT, COCAMIDE MEA, FRAGRANCE (PARFUM), GLYCERIN, LAURYL/MYRISTYL AMIDOPROPYL AMINE OXIDE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, PEG-120 METHYL GLUCOSE DIOLEATE, SODIUM CHLORIDE, SODIUM SULFATE, TETRASODIUM EDTA, WATER (AQUA), YELLOW 5 (CI 19140), ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT

LABEL COPY

IMAGE OF THE LABEL

CVS PHARMACY  CITRUS FRESH
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-725
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
TANGERINE PEEL (UNII: JU3D414057)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM SULFATE (UNII: 0YPR65R21J)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
GINGER (UNII: C5529G5JPQ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-725-641892 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/13/2014
Labeler - CVS PHARMACY (062312574)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(59779-725)

Revised: 1/2014
Document Id: 1ca2c406-0c2d-416e-aada-d48e091ba985
Set id: ebc38725-4303-4e1f-a794-ee0550af967b
Version: 1
Effective Time: 20140114
 
CVS PHARMACY