HAND SANITIZER GEL HAND RX- ethyl alcohol gel

Hand Sanitizer Gel by

Drug Labeling and Warnings

Hand Sanitizer Gel 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 ingredients purpose

Ethyl Alcohol 70% Antiseptic

PURPOSE

Uses

• 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 - hands

Flammable. Keep away from heat 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 recommended for infants

STORAGE AND HANDLING

Other information

• do not store above 105F
• may discolor some fabrics
• harmful to wood finishes and plastics

INACTIVE INGREDIENT

Inactive ingredients water, glycerin, propylene glycol, carbomer, fragrance

PRINCIPAL DISPLAY PANEL

Hand Rx

Hand Sanitizer Gel

70% Alcohol

Advanced formula Clean Scent

Net Contents: 1 Gallon (3.78L)

PRINCIPAL DISPLAY PANEL

Hand Rx

Hand Sanitizer Gel

70% Alcohol

Advanced formula Clean Scent

Net Contents: 1 Gallon (3.78 L)

INGREDIENTS AND APPEARANCE

HAND SANITIZER GEL  HAND RX
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-585
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-585-01	3.78 L in 1 BOTTLE; Type 0: Not a Combination Product	07/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/17/2020

Labeler - Blue Cross Laboratories, Inc. (008298879)

Registrant - Blue Cross Laboratories, Inc. (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Blue Cross Laboratories, Inc.		008298879	manufacture(22431-585)