Active Ingredient
Active Ingredients: Ethyl Alcohol 80%
Pharmacys Prescription Hand Sanitizer
FDA Label NDC 72197-023
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by American Consumer Products Corp for the product Pharmacys Prescription Hand Sanitizer (NDC 72197-023). 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 active ingredient, purpose, warnings, indications & usage section, stop use, keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Purpose: Antiseptic
Uses - Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
Warnings - For external use only. Do not swallow.
Flammable. Keep away from fire or flame.
Do not apply around eyes. Do not use in ears & mouth.
Indications & Usage Section
When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
Stop Use
Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.
Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions - Spray directly onto hands, rub into skin until dry. Spray directly onto surfaces: knobs, handles, steering wheels, light switches, grocery carts, countertops, etc and let air dry.
Other Information
Other information - store at 20° C (68° to 77° F).
- may discolor fabrics.
Inactive Ingredients
INACTIVE INGREDIENTS: Purified Water (Aqua), Glycerin, Hydrogen Peroxide.
Distributed By
Distributed By:
American Consumer Products Corp
Vernon, CA 90058
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