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Aterra7 antibacterial foaming hand - Medication Information

Product NDC Code 68306-115
Drug Name

Aterra7 antibacterial foaming hand

Type Brand
Active Ingredients
Benzalkonium chloride 1 mg/ml
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 1233282
Application Number 505G(a)(3)
Labeler Name B4 Ventures LLC
Packages
Package NDC Code Description
68306-115-01 530 ml in 1 bottle, pump (68306-115-01)
68306-115-02 4 bag in 1 box (68306-115-02) / 1000 ml in 1 bag
68306-115-03 4 bottle, pump in 1 box (68306-115-03) / 1000 ml in 1 bottle, pump
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzalkonium Chloride 0.1%

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 Apply a palmful to hands and forearms. Scrub thoroughly for at least 15 seconds. Rinse completely and dry.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Fragrance

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.
Use reduces amount of bacteria on hands

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Aterra7 Antibacterial Foaming Hand Benzalkonium Chloride WATER BENZALKONIUM CHLORIDE BENZALKONIUM LAURAMINE OXIDE GLYCERIN PEG-120 METHYL GLUCOSE DIOLEATE 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.
Product Label - 1000 mL Cartridge - Front Product Label - 1000 mL Cartridge - Back

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.

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 . When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition 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