BLUE DEVIL HAND SANITIZER- alcohol solution

Blue Devil Hand Sanitizer by

Drug Labeling and Warnings

Blue Devil Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Blue Cross Laboratories, Ningbo Liyuan Daily Chemical Products Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 62% Purpose: Antiseptic

Purpose

Uses

• to decrease bacteria on the skin
• recommended for repeated use

Warnings

For external use only-hands. Flammable. Keep away from heat or flame

Do not use

• not recommended for infants

INDICATIONS & USAGE

• avoid contact with broken skin
• do not inhale or ingest

WHEN USING

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor if

• skin irritation develops

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.

Directions

• wet hands thoroughly with product and allow to dry without wiping.
• for children under 6, use only under adult supervision
• not recommended for infants

Inactive ingredients

water, glycerin, propylene glycol, carbomer

Package Label - Principal Display Panel

Blue Devil

Hand Sanitizer

Fights 99.99% of germs and bacteria

Helps stop the spread of illness

Great for travel, home, & workplace

8oz. 237ml part #00245

INGREDIENTS AND APPEARANCE

BLUE DEVIL HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-222
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-222-01	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/13/2020

Labeler - Blue Cross Laboratories (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd		530766098	manufacture(22431-222)