HAND SANITIZER- alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by True Value Company, L.L.C., TV GPMC, L.L.C.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Directions: Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

WARNINGS

Warnings. For external use only. Flammable. Keep away from heat or flame. Do not use in children less than 2 months of age on open skin wounds When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Inactive ingredients: glycerin, hydrogen peroxide, purified water USP

INDICATIONS & USAGE

Use[s]: Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

ACTIVE INGREDIENT

Active ingredient[s] : Isopropyl alcohol 75% v/v

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

PURPOSE

Purpose: Antiseptic

PRINCIPAL DISPLAY PANEL

tion Antiseptic Hand Rub Non-sterile Solution

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73998-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73998-001-02	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
2	NDC: 73998-001-04	1892 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
3	NDC: 73998-001-03	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/26/2020

Labeler - True Value Company, L.L.C. (006929681)

Registrant - True Value Company, L.L.C. (006929681)

Establishment
Name	Address	ID/FEI	Business Operations
True Value Company, LLC		006929681	manufacture(73998-001)