HAND RX HAND SANITIZER- alcohol solution

Hand Rx Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient(s)

Alcohol 62% v/v. Purpose: Antiseptic

PURPOSE

Antiseptic

Use

• to reduce bacteria on the skin that could cause disease.
• recommended for repeat use.

Warnings

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

Do not use

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

Other information

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

Inactive ingredients

water, glycerin, propylene glycol, carbomer

Package Label - Principal Display Panel

Hand Rx Hand Sanitizer Antiseptic Solution

8 FL OZ. (236 ml)

INGREDIENTS AND APPEARANCE

HAND RX HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-221
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
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-221-01	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/11/2020

Labeler - Blue Cross Laboratories (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd		530766098	manufacture(22431-221)