ADVANCED HAND SANITIZER- ethyl alcohol 70% liquid
Kareway Product, Inc.

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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Pure-Aid Advanced Hand Sanitizer

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria on skin

Warnings

Flammable, Keep away from fire or flame.

For external use only.

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

irritation or rash appears and lasts

Keep out of reach of children

If swallowed, get medical help or contact or contact a Poison Control Center right away

Directions

Put enough product in your palm to cover hands and rub hands together briskly until dry
Children under 6 years of age should be supervised when using this product.

Other Information

Store below 110ºF (43ºC)

Inactive Ingredients

Water (Aqua), Aminomethyl Propano, Carbomer, Citrus Aurantium Dulcis (Orange) Fruit Extract, Fragrance, Propylene Glycol, 1,2-Hexanediol, Denatonium Benzoate

Principal Display Panel

label

ADVANCED HAND SANITIZER
ethyl alcohol 70% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67510-0132
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)
ORANGE OIL (UNII: AKN3KSD11B)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:67510-0132-8	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
2	NDC:67510-0132-1	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/30/2020

Labeler - Kareway Product, Inc. (121840057)