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Avant Original Fragrance Free Prescribing Information

Package insert / product label
Generic name: alcohol gel
Dosage form: hand sanitizer
Drug class: Antiseptic and germicides

Medically reviewed by Drugs.com. Last updated on Dec 1, 2023.

Drug Facts

Active Ingredient

Ethanol 60%

Purpose

Antimicrobial

Indications and Usage for Avant Original Fragrance Free

  • Hand sanitizer to help reduce bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only.

Flammable, keep away from fire or flame.

When using this product do not use in or near eyes. In case of eye contact, flush thoroughly with water.

Stop use and ask doctor if irritation and redness develop and persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Avant Original Fragrance Free Dosage and Administration

  • Dispense an adequate amount in your palm to cover all surfaces of hands completely
  • Rub hands together until dry
  • Supervise children in the use of this product

Other Information

  • Do not store above 100 ºF (38 ºC)
  • May discolor some fabrics

Inactive Ingredients

Water, Propylene Glycol, Triethanolamine, Carbomer, Glycerin

Questions or Comments?

1-888-667-6066 or www.b4brands.com

Front Label - 1 GallonBack Label - 1 Gallon

AVANT ORIGINAL - FRAGRANCE FREE
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68306-106
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68306-106-02500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/15/2010
2NDC:68306-106-0182.5 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/15/201003/31/2023
3NDC:68306-106-031000 mL in 1 POUCH; Type 0: Not a Combination Product05/15/2010
4NDC:68306-106-0460 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/15/2010
5NDC:68306-106-05120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/15/201011/30/2023
6NDC:68306-106-061920 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/2010
7NDC:68306-106-083785 mL in 1 JUG; Type 0: Not a Combination Product05/15/2010
8NDC:68306-106-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product05/01/2012
9NDC:68306-106-1159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2020
10NDC:68306-106-12251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/15/2010
11NDC:68306-106-09208198 mL in 1 DRUM; Type 0: Not a Combination Product04/04/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/15/2010
Labeler - B4 Ventures LLC (133582853)

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