Barolon Hand Sanitizer
FDA Label NDC 76723-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Barolon Labs for the product Barolon Hand Sanitizer (NDC 76723-100). 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 drug facts, active ingredients, purpose, use:, warnings:, otc - 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
Active Ingredients
Ethyl Alcohol 70% v/v
Purpose
Antimicrobial
Use:
Hand sanitizer to help reduce bacteria on skin.
Warnings:
Flammable. Keep away from fire or flame.
For external use only.
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Directions:
Put enough product in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using.
Other Information:
Store below 110°F (43°C)
Inactive Ingredients:
Water (Aqua), Aloe Barbadensis Leaf Juice, Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Tocopherol Acetate.
Other
MADE WITH PLANT EXTRACTS AND SKIN CONDITIONERS
HIGH POTENCY 70% ALCOHOL FORMULA
Dist By: BAROLON INC. SOUTH HOLLAND, IL 60473
* Please review the disclaimer below.
