HAND SANITIZER HAND RX- ethyl alcohol liquid 
Blue Cross Laboratories, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hand Rx Hand Sanitizer

Active ingredients       purpose

Ethyl Alcohol 62%       Antimicrobial        

Kills over 99% of most common germs

Keep out of reach of children

Keep out of eyes.In case of eye contact immediately flush eyes with water then contact physician.

Warning: flammable. Keep away from flame. If swallowed, contact physician. For external use only. Do not store above 110 degrees farenheit.

directions:

put a thumbnail size amount in your palm and rub your hands together briskly until dry

Children under 6 years of age should be supervised when using Hand Rx.

Inactive Ingredients: Water, Glycerin, Propylene Glycol, Carbomer

Hand Rx

Hand Sanitizer

Kills 99.99% of germs

8 Fl Oz. (236 ml)

back label

front label

HAND SANITIZER  HAND RX
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-581
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22431-581-01236 mL in 1 BOTTLE; Type 0: Not a Combination Product10/12/2010
2NDC:22431-581-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product10/12/2010
3NDC:22431-581-03118 mL in 1 BOTTLE; Type 0: Not a Combination Product10/12/2010
4NDC:22431-581-041180 mL in 1 BOTTLE; Type 0: Not a Combination Product10/12/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/12/2010
Labeler - Blue Cross Laboratories, Inc. (008298879)
Registrant - Blue Cross Laboratories, Inc. (008298879)
Establishment
NameAddressID/FEIBusiness Operations
Blue Cross Laboratories, Inc.008298879manufacture(22431-581)

Revised: 7/2020
Document Id: aa1974ce-90c6-f671-e053-2a95a90a697b
Set id: 76d74b1b-ed40-4525-8556-b7a0485a75cb
Version: 13
Effective Time: 20200710
 
Blue Cross Laboratories, Inc.