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Qc 8oz instant hand sanitizer (original) - Medication Information

Product NDC Code 76176-035
Drug Name

Qc 8oz instant hand sanitizer (original)

Type Brand
Active Ingredients
Alcohol 62 ml/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581660
Application Number part333A
Labeler Name Ningbo Liyuan Daily Chemical Products Co., Ltd.
Packages
Package NDC Code Description
76176-035-01 236 ml in 1 bottle, plastic (76176-035-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Medicinal Ingredient Ethyl Alcohol 62%

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 rub until dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Non-Medicinal Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Parfum, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

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.
Features To decrease bacteria on the skin that could cause disease. Recommended for repeated use. Use anywhere without 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.
QC 8OZ INSTANT HAND SANITIZER (ORIGINAL) ALCOHOL ALCOHOL ALCOHOL WATER

Animal pharmacology and or toxicology

Information from studies of the drug in animals, if the data were not relevant to nor included in other parts of the labeling. Most labels do not contain this field.
This product was not tested on animals

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.
Other information Do not store above 105℉. May discolor some fabrics. Harmful to wood finishes and plastics. 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 of children. In case of accidental ingestion, seek professional assistance or contact a Posion Control Center immediately.

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 Keep out of eys. In case of contact with eyes, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin.

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.
Warning For external use only-hands Flammable, keep away from heat and flame Discontinue if skin becomes irritated and ask a doctor

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