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CVS PHARMACY COCONUT WATER by CVS PHARMACY

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: CVS PHARMACY
NDC Code: 59779-842

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

Use
  • Helps eliminate bacteria on the skin.

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
  • Apply onto dry hands. Work into a lather, rinse and dry thoroughly.

Other information
  • Store at room temperature.

Inactive ingredients

Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Cocos Nucifera (Coconut) Fruit Extract, Bambusa Vulgaris Extract, Propylene Glycol, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).

Label Copy

CVS PHARMACY  COCONUT WATER
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-842
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
COCAMIDOPROPYL BETAINE 
POLYSORBATE 20 
GLYCERIN 
DECYL GLUCOSIDE 
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) 
ALOE VERA LEAF 
COCONUT 
BAMBUSA VULGARIS TOP 
PROPYLENE GLYCOL 
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) 
EDETATE SODIUM 
SODIUM CITRATE 
CITRIC ACID MONOHYDRATE 
SULISOBENZONE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:59779-842-08222 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/26/2018
Labeler - CVS PHARMACY (062312574)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(59779-842)

 
CVS PHARMACY

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Medically reviewed on Apr 27, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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