Active Ingredient
Active Ingredients: Ethyl Alcohol 75%
Pharmacys Prescription Hand Sanitizer
FDA Label NDC 72197-035
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 72197-035). 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, stop use, keep out of reach of children, inactive ingredients, directions, indications & usage section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Purpose: Antiseptic
Uses - Reduces bacteria on skin that could cause disease.
Warnings
Warnings - For external use only. Do not ingest or swallow.
Flammable. Keep away from fire or flame.
Stop Use
Stop use and ask a doctor if: If redness or irritation develops and persists for more than 72 hours.
Keep Out Of Reach Of Children
Keep out of reach of children. Do not use on children less than 2 months of age. If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredients
Inactive ingredients - Glycerin, propylene glycol, triethanolamine, carbomer, fragrance, disodium edta, tocopheryl acetate, deionized water.
Directions
Directions: apply as needed in your palms, rub into skin until dry.
Indications & Usage Section
When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
Pharmacy's Prescription Label
Pharmacys Prescription Hand Sanitizer (Acp Ndc 72197 035 10 Pen Hand Sanitizer 070221)
* Please review the disclaimer below.
