7T ALCOHOL HAND SANITIZER- ethyl alcohol liquid 
Avmor

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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63937-2195

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic.

Uses

  • Kills harmful bacteria/germs.
  • For personal hand hygiene to help prevent the spread of bacteria.

Warnings

  • For external use only.
  • Flammable, keep away from fire or flame.

When using this product

  • Avoid contact with eyes. Should this occur, flush eyes with water.

  • If irritation and redness develops.
  • If swallowed, call poison control centre or get medical help right away.

Keep out of reach of children

Directions

  • Use as needed.
  • Apply a minimum of 0.4 ml (0.01 oz) of sanitizer into the palm of your hand. Rub product onto hands for at least 30 seconds and allow to dry.
  • For children under 11, use only under adult supervision.

Other Information

  • Store in a cool, dry place below 40 °C (104 F)

Inactive Ingredients

  • Water (Aqua), Denatonium Benzoate Anhydrous, Carbomer, triethanolamine, Glycerin

Questions?

950, Michelin, Laval, Quebec,Canada H7L5C11 800 387-8074.   www.avmor.com

Avmor®

7T ALCOHOL HAND SANITIZER

Product certified for reduced environmental impact. View specific attributes evaluated: UL.com/EL

473ml (16 US fl oz)

7T 473mL Label

7T ALCOHOL HAND SANITIZER 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63937-2195
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
TROLAMINE (UNII: 9O3K93S3TK)  
POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63937-2195-112 in 1 BOX03/13/2020
1473 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/13/202003/13/2020
Labeler - Avmor (202107827)
Establishment
NameAddressID/FEIBusiness Operations
Avmor202107827manufacture(63937-2195) , label(63937-2195) , pack(63937-2195)

Revised: 9/2021
Document Id: cc0c8bd5-b1dd-11af-e053-2995a90a5efd
Set id: 47ed2a69-e277-46f3-b0ff-4dd1982fc9a7
Version: 2
Effective Time: 20210915
 
Avmor