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Reddy lab advanced alcohol gel sanitizer - Medication Information

Product NDC Code 79671-797
Drug Name

Reddy lab advanced alcohol gel sanitizer

Type Brand
Active Ingredients
Alcohol .7 ml/ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581662
Application Number 505G(a)(3)
Labeler Name Flavor Reddy Foods, LLC
Packages
Package NDC Code Description
79671-797-04 3780 ml in 1 jug (79671-797-04)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Ethyl Alcohol 70%

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 Read the entire label before using this product. Place enough product on your palm to thoroughly cover your hands. Rub hands together briskly until dry.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Water, Glycerin, PEG-6 (and) AMP - Acrylates/Vinyl Isodecanoate Crosspolymer, Diisopropanolamine, Aloe Barbadensis Leaf Juice.

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 reduce microorganisms on the skin Use thi product when soap and water are not available

Purpose

Information about the drug product’s indications for use.
Anitseptic

Spl product data elements

Usually a list of ingredients in a drug product.
Reddy Lab Advanced Alcohol Gel Sanitizer Alcohol WATER DIISOPROPANOLAMINE ALOE VERA LEAF POLYETHYLENE GLYCOL, UNSPECIFIED ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) ALCOHOL ALCOHOL 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.
Display Panel 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

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.
Wanings For external use only. Do not ingest Avoid contact with eyes. If contact occurs, rinse thoroughly with water. FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition. Discontinue use if irritation or redness develops. If irritation persists for more than 72 hours, contact a physician. KEEP OUT OF THE REACH OF CHILDREN IF swallowed, get medical help or contact a Poison Control Center right away.

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