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U instant hand sanitizer classic 2oz - Medication Information

Product NDC Code 52000-201
Drug Name

U instant hand sanitizer classic 2oz

Type Brand
Active Ingredients
Alcohol 62 ml/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581660
Application Number part333A
Labeler Name Universal Distribution Center LLC
Packages
Package NDC Code Description
52000-201-01 60 ml in 1 bottle, plastic (52000-201-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active Ingredient Ethyl Alcohol 62.0 percent

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 Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS: Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), triethanolamine.

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 skin.

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.
U INSTANT HAND SANITIZER CLASSIC 2OZ Ethyl Alcohol PROPYLENE GLYCOL .ALPHA.-TOCOPHEROL ACETATE ALOE VERA LEAF CARBOMER 934 TRIETHANOLAMINE BENZOATE GLYCERIN WATER 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.
label

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 for children. If swallowed, get medical help or contact a Poison Control Center right away.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts.

Storage and handling

Information about safe storage and handling of the drug product.
Other Information: Store below 106 Fahrenheit (41 Degree Celsius) May discolor certain fabrics or surfaces.

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 Flammable. Keep away from fire or flame. For external use only.

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