Otc - Active Ingredient
Active Ingredient:
Benzethonium Chloride 0.105%
Hand Sanitizer
FDA Label NDC 72131-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rimports Inc. for the product Hand Sanitizer (NDC 72131-004). 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, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, other safety information, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Otc - Stop Use
Stop use and ask a doctor if redness appears and persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN. If swallowed, contact medical help or poison control.
Dosage & Administration
Directions Spray on palm and rub your hands together until absorbed.
Inactive Ingredient
Inactive Ingredients
Water, PEG-40 Hydrogenated Castor Oil, Betaine, Fragrance, Citrus Limon (Lemon) Peel Oil, Citrus Grandis (Grapefruit) Peel Oil, Phenoxyethanol, Diazolidinyl Urea, Palmitamidopropyltrimonium Chloride, Sodium Citrate, Disodium EDTA.
Other Safety Information
Other Information
May damage fabrics and surfaces.
Indications & Usage
Uses
For waterless hand washing to decrease bacteria on skin. Recommended for repeated use.
Warnings
WARNINGS:
For external use only.
Otc - When Using
When using this product, Avoid face, eyes or sensitive areas. If contact occurs flush thoroughly with water.
* Please review the disclaimer below.
