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Foaming hand sanitizer - Medication Information

Product NDC Code 75044-280
Drug Name

Foaming hand sanitizer

Type Brand
Active Ingredients
Benzalkonium chloride 1.3 g/1000ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1020365
Application Number M003
Labeler Name American Chemical Systems II, LLC
Packages
Package NDC Code Description
75044-280-16 2 bottle, plastic in 1 case (75044-280-16) / 3800 ml in 1 bottle, plastic
75044-280-31 3 bottle, plastic in 1 case (75044-280-31) / 1000 ml in 1 bottle, plastic
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active ingredient Benzalkonium chloride .13%.......Antibacterial

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 • wet hands thoroughly with product and allow to dry without wiping • supervise children when using this product

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Purified Water, Aloe Vera, Propylene Glycol, Triethylene Glycol, Polysorbate-20, 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.
Uses • hand sanitizer to decrease bacteria on the skin

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Foaming Hand Sanitizer Hand Sanitizer BENZALKONIUM CHLORIDE BENZALKONIUM WATER ALOE VERA FLOWER PROPYLENE GLYCOL TRIETHYLENE GLYCOL POLYSORBATE 20

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.
ACS™ FOAMING HAND SANITIZER Labeling ACS™ FOAMING HAND SANITIZER Distributed by: AMERICAN CHEMICAL SYSTEMS II, LLC 2520 South Sheridan St., Wichita, Kansas 67217 (800) 889-3489 Lot No: Expiry Labeling [2 x 1 gal. (7.6 L)] Labeling [3-33.8 fl oz (1 L) Bottles (101.4 fl oz (3 qt 5.4 fl oz) (3 L))] rege ACS 26116 3- per Box ACS 26116 1000 mL Botl ACS 26116 2-per box 1 Gal Botl

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 • do not get into eyes. In case of contact, rinse eyes thoroughly with water Stop use and ask a doctor if • irritation or redness develop and condition persists.

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