ADVANCED HAND SANITIZER- alcohol gel

Advanced Hand Sanitizer by

Drug Labeling and Warnings

Advanced Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Blue Cross Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient(s)

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

PURPOSE

Use

• To decrease bacteria on the skin that could cause disease.
• recommended for repeated use

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.

INDICATIONS & USAGE

Stop use and ask a doctor if

• Skin irritation develops

WARNINGS

Warnings

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

When using this product

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with broken skin
• Do not inhale or ingest

DOSAGE & ADMINISTRATION

Directions

• Wet hands thoroughly with product and allow to dry without wiping
• For children under 6, use only under adult supervision
• not recommend for infants

STORAGE AND HANDLING

Other information

• do not store above 105ºF
• may discolor some fabrics
• harmful to wood finishes and plasics

INACTIVE INGREDIENT

Inactive ingredients water, glycerin, propylene glycol,carbomer

PRINCIPAL DISPLAY PANEL

Royalty Premier

Advanced

Hand Sanitizer

Fights Germs and Bacteria

40 FL OZ (1.18 L)

INGREDIENTS AND APPEARANCE

ADVANCED HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-254
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-254-01	1.18 L in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/17/2020

Labeler - Blue Cross Laboratories, Inc (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Blue Cross Laboratories, Inc		008298879	manufacture(22431-254)