Active Ingredient
Active Ingredients - Ethyl Alcohol 65%
Pharmacys Prescription Hand Sanitizer
FDA Label NDC 72197-022
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 72197-022). 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, uses, warnings, otc - when using, stop use and ask a doctor, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
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 appy around eyes. Do not use in ears & mouth.
Otc - When Using
When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
Stop Use And Ask A Doctor
Stop use and ask a doctor if redness or irritation develops and persists more than 72 hours.
Otc - 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 - pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.
Other Information
Other information - store at 20° C (68° to 77° F). May discolor fabrics.
Inactive Ingredient
INACTIVE INGREDIENTS: Purified Water (Aqua), Carbomer, Aminomethyl Propanol, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis (Aloe Vera) Leaf Juice
* Please review the disclaimer below.
