ANTISEPTIC HAND RUB- alcohol liquid

Antiseptic Hand Rub by

Drug Labeling and Warnings

Antiseptic Hand Rub by is a Otc medication manufactured, distributed, or labeled by ChemQuest Chemicals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient(s)

• Active Ingredient: Purpose
• Ethyl Alcohol 72% v/v.: Antiseptic

Purpose

Antiseptic, Hand Rub

Use[s]

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

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.

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

• Store between 15-30°C (59-86°F)
• Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

aloe vera, FD&C Blue #1, FD&C Yellow #5, fragance, tocopheryl acetate (vitamin E), propylene glycol, purified water USP

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ANTISEPTIC HAND RUB 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77441-1000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	7200 L  in 10000 L

Inactive Ingredients
Ingredient Name	Strength
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77441-1000-1	1249.18596 L in 1 DRUM; Type 0: Not a Combination Product	05/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/18/2020

Labeler - ChemQuest Chemicals LLC (835052051)

Registrant - ChemQuest Chemicals LLC (835052051)

Establishment
Name	Address	ID/FEI	Business Operations
ChemQuest Chemicals LLC		835052051	manufacture(77441-1000) , pack(77441-1000) , label(77441-1000)