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

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AVID HAND SANITIZING WIPE  70 PERCENT
ethyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72580-311
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
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
LEMON OIL (UNII: I9GRO824LL)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72580-311-111 mL in 1 POUCH; Type 0: Not a Combination Product11/19/202011/19/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00311/19/202011/19/2021
Labeler - Formology Lab Inc. (081102403)

Revised: 1/2024
 

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