FREE HAND SANITIZER- alcohol gel

FREE Hand Sanitizer by

Drug Labeling and Warnings

FREE Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by BLAKEMORE SALES CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

• helps reduce bacteria that potentially can cause disease
• helps prevent cross contamination by hand contact
• recommended for repeated use

Warnings

For external use only.

Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age or on open skin wounds

When using this product

• keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or redness develops.

Keep out of reach of children.

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

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.

Other information

• avoid freezing and excessive heat above 40°C(104°F)
• may disolor certain fabrics

Inactive ingredients

Water, Glycerin, Aloe Barbadensis Extract, Aminomethyl Propanol, Propylene Glycol, Carbomer, Fragrance, Tocopherol.

Package Labeling

INGREDIENTS AND APPEARANCE

FREE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78304-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78304-005-01	500 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package	05/22/2020	01/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/22/2020	01/31/2026

Labeler - BLAKEMORE SALES CORPORATION (164380578)