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Hand sanitizer - Medication Information

Product NDC Code 79091-008
Drug Name

Hand sanitizer

Type Brand
Active Ingredients
Alcohol 70 mg/ml
Route TOPICAL
Dosage Form SPRAY
Application Number 505G(a)(3)
Labeler Name HAAN BRAND SL
Packages
Package NDC Code Description
79091-008-01 30 ml in 1 bottle, spray (79091-008-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Active Ingredient Purpose Ethyl Alcohol 65%...................................Antiseptic

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 Directions: Wet hands throughly with product and allow to dry without wiping For Children under 6 years of age do not use without supervision of an adult. Not recomended for infants

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water, C10-30 Alkyl Acrylate Crosspolymer, Parfum(Fragrance), Limonene, Tromethamine, Linalool, potassium Sorbate, Geraniol, Sodium Benzoate Back Label

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 Uses * To decrease bacterias on the hand. Recommended for repeated use.

Purpose

Information about the drug product’s indications for use.
Uses Uses * To decrease bacterias on the hand. Recommended for repeated use.

Spl product data elements

Usually a list of ingredients in a drug product.
Hand Sanitizer Alcohol ALCOHOL ALCOHOL SODIUM BENZOATE CARBOMER 934 METHYL GLUCETH-10 WATER GERANIOL ALOE VERA LEAF LINALOOL, (+)- POTASSIUM SORBATE BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER TROMETHAMINE

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.
Hand Sanitizer Gel Front 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 Keep out of reach of children. In case of incidental ingestion, see professional advice or contact a Poison Control Center inmediately.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? QUESTIONS OR COMMENTS: Visit Haanready.com

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if Stop use and ask a doctor if * Irritation develops

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- hands When using this product keep out o f eyes. In case of contact, flush throughly with water. Do Not Inhale or ingest. Avoid contact with broken skin Keep out of reach of children. In case of incidental ingestion seek professional assistance or contact a Poison Control Center inmediately. Stop use and ask Doctor: if skin irritation develops. Flammable: Keep away from heat and flame.

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