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.

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DRUG FACTS

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

Warnings

For external use only.

When using this product

  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop using this product and ask doctor if

  • irritation and redness develop and last.

Keep out of reach of children

  • In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

Other information

Inactive ingredients

Aloe Barbadensis Leaf Juice, Blue 1 (CI 42090), Camellia Sinensis Leaf Extract, Citric Acid, Cocamidopropyl Betaine, Decyl Glucoside, Fragrance (Parfum), Glycerin, Methylchloroisothiazolinone, Methylisothiazolinone, Polyquaternium-7, Polysorbate 20, Red 33 (CI 17200), Sodium Citrate, Tetrasodium EDTA, Water (Aqua), Xanthan Gum

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 MONOHYDRATE (UNII: 2968PHW8QP)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
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:59779-842-31946 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/09/2016
Labeler - CVS PHARMACY (062312574)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(59779-842)

Revised: 2/2016
Document Id: e6e0aa6a-56cb-4cb1-a59e-df1fef8f7c55
Set id: c31fd094-9f4d-4154-a1a3-ffbcd4243a41
Version: 3
Effective Time: 20160210
 
CVS PHARMACY