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CAREONE Antibacterial Sanitizer Fresh Water

Medically reviewed on April 26, 2017

Dosage form: liquid
Ingredients: ALCOHOL 650mg in 1mL
Labeler: American Sales Company
NDC Code: 41520-412

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

Ethyl Alcohol 65%

Purpose

Antiseptic

Uses

to decrease bacteria on the skin.

Warnings

For external use only.

  • Flammable
  • Keep away from source of heat or fire

When using this product

avoid contact with eyes. If contact occurs, rinse 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
  • put enough product in your palm to cover hands and rub hands together until dry.
  • children under 6 years should be supervised when using this product

Inactive ingredients

Water (Aqua), Fragrance (Parfum), Carbomer, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Synthetic Wax, Microcrystalline Wax, Tocopheryl Acetate, Hydroxypropyl Methylcellulose, Blue 1 Lake (CI 42090), Yellow 5 (CI 19140).

Label Copy

CAREONE  ANTIBACTERIAL SANITIZER FRESH WATER
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41520-412
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL650 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CARBOMER 934 
GLYCERIN 
ISOPROPYL ALCOHOL 
ISOPROPYL MYRISTATE 
AMINOMETHYLPROPANOL 
ALOE VERA LEAF 
SYNTHETIC WAX (1800 MW) 
MICROCRYSTALLINE WAX 
.ALPHA.-TOCOPHEROL ACETATE, DL- 
HYPROMELLOSES 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:41520-412-0359 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/25/2017
Labeler - American Sales Company (809183973)
Registrant - Apollo Health and Beauty Care Inc. (201901209)
Establishment
NameAddressID/FEIOperations
Apollo Health and Beauty Care Inc.201901209manufacture(41520-412)

 
American Sales Company

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Further information

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

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