7T FOAMING 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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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), 2-propanol, Bis-PEG-12 Dimethicone, Cetyl Alcohol, Denatonium Benzoate

Questions?

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

Avmor®

7T FOAMING ALCOHOL HAND SANITIZER

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

250 ml (8.5 US fl oz)

NEW-2198-225ML-7T FOAMING SANITIZER_1

NEW-2198-225ML-7T FOAMING SANITIZER_2

NEW-2198-225ML-7T FOAMING SANITIZER_4

7T FOAMING ALCOHOL HAND SANITIZER
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63937-2198
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)
CETYL ALCOHOL (UNII: 936JST6JCN)
DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:63937-2198-4	12 in 1 BOX	05/05/2020
1		225 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	05/05/2020	05/05/2020

Labeler - Avmor (202107827)

Name	Address	ID/FEI	Business Operations
Establishment
Avmor		202107827	manufacture(63937-2198) , label(63937-2198) , pack(63937-2198)

Revised: 1/2022

Document Id: d58d0489-54b3-461f-e053-2995a90a1f35

Set id: a4e8c29a-5a1b-6d62-e053-2995a90a39e6

Version: 2

Effective Time: 20220114

Avmor