ONE TOUCH HAND SANITIZER- alcohol gel 
One Touch Medical 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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One Touch Hand Sanitizer Gel

One Touch Hand Sanitizer Gel

Drug Facts

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

When using this product

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Directions

Inactive ingredients

Aloe barbadensis extract, Purified water, Aminomethyl Propanol, Carbomer, Glycerin

Active ingredient

Alcohol 70% v/v

Do not use

Do not use

Package Label - Principal Display Panel

LabelMade in Canada

Label

Label

Label

Label

Label

LabelLabel

ONE TOUCH HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77301-604
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ALOE (UNII: V5VD430YW9)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77301-604-5160 mL in 1 BOTTLE; Type 0: Not a Combination Product05/19/2020
2NDC:77301-604-52250 mL in 1 BOTTLE; Type 0: Not a Combination Product05/19/2020
3NDC:77301-604-53500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/19/2020
4NDC:77301-604-541000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/19/2020
5NDC:77301-604-5519000 mL in 1 PAIL; Type 0: Not a Combination Product05/19/2020
6NDC:77301-604-563790 mL in 1 JUG; Type 0: Not a Combination Product07/07/2020
7NDC:77301-604-573790 mL in 1 JUG; Type 0: Not a Combination Product07/07/2020
8NDC:77301-604-58208198 mL in 1 DRUM; Type 0: Not a Combination Product07/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/19/2020
Labeler - One Touch Medical Inc (204124713)
Registrant - One Touch Medical Inc (204124713)

Revised: 7/2020
Document Id: aaada9fe-951c-3960-e053-2995a90ad178
Set id: a60708b5-f199-20dd-e053-2a95a90a16cf
Version: 3
Effective Time: 20200717
 
One Touch Medical Inc