HAND SANITIZER LEMON SCENT HAND RX- ethyl alcohol gel 
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 Lemon Scent

Active ingredient              Purpose

Ethyl Alcohol  62.0%        Antimicrobial

Uses hand sanitizer to help reduce bacteria on the skin that may cause disease

keep out of reach. If swallowed, get medical help or contact a Poison Control Center.

Stop use and ask a doctor if irritation or redness develops

Warnings

For external use only

Flammable. Keep away from heat and flame.

When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Directions

wet hands thoroughly with product and rub into skin until dry

Children under 6 years of age should be supervised by an adult when using this product.

Inactive Ingredients water (aqua), triethanolamine, carbomer, aloe barbadensis leaf juice, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E).


Hand Rx

Hand Sanitizer

Kills 99.99% of Germs

Leaves Hands Feeling Soft

Lemon Scent

2 FL OZ (59 mL)

package

Bottle

HAND SANITIZER LEMON SCENT  HAND RX
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-132
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)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22431-132-022 in 1 BLISTER PACK08/19/2014
1NDC:22431-132-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/19/2014
Labeler - Blue Cross Laboratories, Inc. (008298879)
Registrant - Blue Cross Laboratories, Inc. (008298879)
Establishment
NameAddressID/FEIBusiness Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd.530766098manufacture(22431-132)

Revised: 1/2017
Document Id: 0fc4ce37-bc88-4011-b41d-7fcce9efec50
Set id: 6354d3e2-df70-4e61-bfaa-7a60bf6ac7eb
Version: 4
Effective Time: 20170127
 
Blue Cross Laboratories, Inc.