FDA.reportPublic FDA data

Avant 70% Alcohol Gel

Manufacturer
B4 Soap LLC
Effective date
2026-03-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:50:42

Label at a glance#

ProductAvant 70% Alcohol Gel
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

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

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Propylene Glycol, Diisopropylamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label - 55 Gallon DrumProduct Label - 55 Gallon Drum

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68306-116-01Avant 70% Alcohol Gel208198 mL in 1 DRUMGEL2081983

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68306-11668306-116-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIISOPROPYLAMINEBR9JLI40NOIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Avant 70% Alcohol GelALCOHOLB4 Soap LLC241f4334-2e88-4f7b-a0c7-c93da9f5086c2026-03-18WarningsExact identifier
ndc (package): 68306-116-01
ndc (product): 68306-116
ndc11 (package): 68306011601
spl id: 4d4ffa75-38db-5fca-e063-6294a90abb97
spl set id: 241f4334-2e88-4f7b-a0c7-c93da9f5086c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.