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Avant foaming hand sanitizer - Medication Information

Product NDC Code 68306-109
Drug Name

Avant foaming hand sanitizer

Type Brand
Active Ingredients
Alcohol 62 ml/100ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 616763
Application Number 505G(a)(3)
Labeler Name B4 Ventures LLC
Packages
Package NDC Code Description
68306-109-01 530 ml in 1 bottle, pump (68306-109-01)
68306-109-02 1000 ml in 1 pouch (68306-109-02)
68306-109-03 1000 ml in 1 cartridge (68306-109-03)
68306-109-05 1040988 ml in 1 container, flexible intermediate bulk (68306-109-05)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Ethanol 62% v/v

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
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.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water, Acrylates/Perfluorohexylethyl Methacrylate Copolymer, Perfluorohexylethyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses Hand sanitizer to help reduce bacteria on the skin Recommended for repeated use

Purpose

Information about the drug product’s indications for use.
Purpose Antimicrobial

Spl product data elements

Usually a list of ingredients in a drug product.
Avant Foaming Hand Sanitizer Alcohol 2-(PERFLUOROHEXYL)ETHANOL WATER ALCOHOL ALCOHOL ALOE VERA LEAF BUTYL ACRYLATE/METHYL METHACRYLATE/PERFLUOROHEXYLETHYL METHACRYLATE COPOLYMER (SALUS AF) GLYCERIN water white - colorless, dispensed as white foam

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Label - Front - 1000 mL Cartridge Package Label - Back - 1000 mL Cartridge

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other Information Do not store above 100 ºF (38 ºC) May discolor some fabrics

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-888-667-6066 or www. b4brands.com

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API