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Aosi healthcare hand sanitizer - Medication Information

Product NDC Code 43473-056
Drug Name

Aosi healthcare hand sanitizer

Type Brand
Active Ingredients
Alcohol 62 ml/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581660
Application Number M005
Labeler Name Nantong Health & Beyond Hygienic Products Inc.
Packages
Package NDC Code Description
43473-056-01 .9 ml in 1 packet (43473-056-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Alcohol, 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: • Put enough product on your palm to cover hands and briskly rub hands together until dry. • For children under 6 years old, use only under adult supervision.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Acrylates/C10-30 alkyl acrylate crosspolymer, Aloe barbadensis leaf juice, Fragrance, Glycerin, Maltodextrin, Propylene glycol, Tocopheryl acetate, Triethanoamine, Water

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 For hand sanitizing to decrease bacteria on the skin without soap and water

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
AOSI HEALTHCARE HAND SANITIZER ALCOHOL WATER GLYCERIN PROPYLENE GLYCOL ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) .ALPHA.-TOCOPHEROL ACETATE, D- MALTODEXTRIN ALOE VERA LEAF TRICLOSAN ALCOHOL ALCOHOL

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.
image description

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use in the eyes Use with caution if allergic to alcohol

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 directly.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Storage below 105°F. May discolor some fabrics. Harmful to wood finishes and plastic

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 heat or flames

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