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CAREONE Instant Hand Sanitizer with Moisturizers and Vitamin E

Medically reviewed on April 26, 2017

Dosage form: liquid
Ingredients: ALCOHOL 700mg in 1mL
Labeler: American Sales Company
NDC Code: 41520-178

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 70%

Purpose

Antiseptic

Uses
  • to help reduce 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 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
  • 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.

Other information
  • store at a temperature below 110°F (43°C)
  • may discolor some fabrics or surfaces

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Carbomer, Aminomethyl Propanol, Fragrance (Parfum).

Label Copy

CAREONE  INSTANT HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41520-178
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
GLYCERIN 
ISOPROPYL MYRISTATE 
ALOE VERA LEAF 
.ALPHA.-TOCOPHEROL ACETATE, DL- 
CARBOMER 934 
AMINOMETHYLPROPANOL 
Packaging
#Item CodePackage Description
1NDC:41520-178-16443 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(41520-178)

 
American Sales Company

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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