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Dr. talbots - Medication Information

Product NDC Code 70797-160
Drug Name

Dr. talbots

Type Brand
Active Ingredients
Alcohol 75 ml/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 1305100
Application Number part333A
Labeler Name Talbots Pharmaceuticals Family Products, LLC.
Packages
Package NDC Code Description
70797-160-01 50 ml in 1 bottle (70797-160-01)
70797-160-02 250 ml in 1 bottle, pump (70797-160-02)
70797-160-03 500 ml in 1 bottle, pump (70797-160-03)
70797-160-04 1000 ml in 1 bottle, pump (70797-160-04)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Ethyl Alcohol 75%

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. For children under 6, use only under adult supervision.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients aqua, glycerin, carbomer, aminomethyl propanol

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.
Use To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Dr. Talbots Ethyl Alcohol WATER ALCOHOL ALCOHOL AMINOMETHYL PROPANEDIOL CARBOMER 934 GLYCERIN

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.
Package Label - Principal Display Panel Principal Display Panel Principal Display Panel Principal Display Panel Principal Display Panel

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.

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 irritation or redness develops, condition persists for more than 72 hours consult a doctor.

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 avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store at normal room temperature May discolor certain fabrics May be harmful to wood finishes and plastics

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 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