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Walgreens - Medication Information

Product NDC Code 0363-5721
Drug Name

Walgreens

Type Brand
Active Ingredients
Alcohol 700 mg/ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581662
Application Number part333A
Labeler Name walgreens
Packages
Package NDC Code Description
0363-5721-04 59 ml in 1 bottle, plastic (0363-5721-04)
0363-5721-02 59 ml in 1 bottle, plastic (0363-5721-02)
0363-5721-03 59 ml in 1 bottle, plastic (0363-5721-03)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
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.
wet hands thoroughly with product and allow to 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.
Isopropyl alcohol, glycerin, isopropyl myristate, tocopheryl acetate, water, PEG 6 AMP-Acrylates/Vinyl Isodecanoate, fragrance, blue 1, violet 2

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.
to decrease bacteria on the skin that could cause disease recommended for repeated use

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Walgreens Ethyl Alcohol ISOPROPYL ALCOHOL GLYCERIN VAT VIOLET 2 MPEG 6000 ACETYL LYSINE FRAGRANCE CLEAN ORC0600327 ISOPROPYL MYRISTATE .ALPHA.-TOCOPHEROL ACETATE FD&C BLUE NO. 1 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.
59 mL

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.
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.
-irritation or redness develops -condition persists for more than 72 hours

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.
-keep out of eyes. In case of contact with eyes, flush thoroughly with water -avoid contact with broken skin -do not inhale or ingest

Storage and handling

Information about safe storage and handling of the drug product.
do not store above 105⁰ F may discolor some fabrics 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.
For external use only-hands Flammable. Keep away from heat and flame. -keep out of eyes. In case of contact with eyes, flush thoroughly with water -avoid contact with broken skin -do not inhale or ingest -irritation or redness develops -condition persists for more than 72 hours 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