AVID HAND SANITIZING WIPE, 70% ETHYL ALCOHOL, 72580-311

AVID HAND SANITIZING WIPE by

Drug Labeling and Warnings

AVID HAND SANITIZING WIPE by is a Otc medication manufactured, distributed, or labeled by Formology Lab Inc., Expackusa, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AVID HAND SANITIZING WIPE 70 PERCENT- ethyl alcohol solution 
Formology Lab Inc.

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AVID HAND SANITIZING WIPE, 70% ETHYL ALCOHOL, 72580-311

ACTIVE INGREDIENT

ETHYL ALCOHOL 70% V/V

PURPOSE

ANTISEPTIC

USES

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.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes 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. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DISCARD USED WIPES IMMEDIATELY TO PREVENT CROSS CONTAMINATION.

DIRECTIONS

• WIPE ALL AREAS OF HANDS UNTIL THEY ARE VISIBLY CLEAN.
• USE ONE OR MORE WIPES AND DISPOSE IN AN APPROPRIATE TRASH CONTAINER.
• LET HANDS AIR DRY.

OTHER INFORMATION

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENTS

Glycerin, Water, Aloe Barbadensis Leaf Juice, Fragrance, Citrus Limon (Lemon) Peel Oil

QUESTIONS?

Call 1-888-575-AVID

WWW.AVIDPRODUCTS.COM

AVID HAND SANITIZING WIPE  70 PERCENT
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72580-311
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LEMON OIL (UNII: I9GRO824LL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72580-311-11	1 mL in 1 POUCH; Type 0: Not a Combination Product	11/19/2020	11/19/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	11/19/2020	11/19/2021

Labeler - Formology Lab Inc. (081102403)

Revised: 1/2024

Document Id: 0bf5b927-3e56-a12e-e063-6394a90a3d78

34390-5

Set id: dfa236d1-a377-478d-8ffd-ed40ee042f2a

Version: 3

Effective Time: 20240101