Avant 70% Alcohol Gel
FDA Label NDC 68306-116

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by B4 Soap Llc for the product Avant 70% Alcohol Gel (NDC 68306-116). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

Uses

  • 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.

Otc - Keep Out Of Reach Of Children

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

Directions

  • 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 °F (38 °C).
  • May discolor some fabrics.

Inactive Ingredients

Water, Glycerin, Carbomer, Propylene Glycol, Diisopropylamine

Questions Or Comments?

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

Package Label.Principal Display Panel

Drum Label (Drum70alcoholgel 01)

Drum Label (Drum70alcoholgel 01)

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