Otc - Active Ingredient
Ethyl Alcohol 70%
Walgreens Gel
FDA Label NDC 0363-5721
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen for the product Walgreens (NDC 0363-5721). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Indications & Usage
- to decrease bacteria on the skin that could cause disease
- recommended for repeated use
Warnings
For external use only-hands
Flammable. Keep away from heat and flame.
Otc - When Using
-keep out of eyes. In case of contact with eyes, flush thoroughly with water
-avoid contact with broken skin
-do not inhale or ingest
Otc - Stop Use
-irritation or redness develops
-condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
- wet hands thoroughly with product and allow to dry without wiping
- for children under 6, use only under adult supervision
- not recommended for infants
Storage And Handling
- do not store above 105⁰ F
- may discolor some fabrics
- harmful to wood finishes and plastics
Inactive Ingredient
Isopropyl alcohol, glycerin, isopropyl myristate, tocopheryl acetate, water, PEG 6 AMP-Acrylates/Vinyl Isodecanoate, fragrance, blue 1, violet 2
* Please review the disclaimer below.
