Active Ingredient
Active Ingredient_____________________________________Purpose Benzalkonium Chloride 0.1% ………………………………..……... Antiseptic |
The following Structured Product Label (SPL) was submitted to the FDA by Handpower Solutions Inc for the product Handpower Cleaner (tm) Hand Sanitizer (NDC 76915-1001). 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:, when using this product, stop use, keep out of reach of children, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Active Ingredient_____________________________________Purpose Benzalkonium Chloride 0.1% ………………………………..……... Antiseptic |
Active Ingredient_____________________________________Purpose
Benzalkonium Chloride 0.1% ………………………………..……... Antiseptic
Uses: Hand sanitizer to help reduce bacteria and other pathogens that potentially can cause disease. For use when soap and water are not available. Not for use on the face or other sensitive areas.
Warnings: FOR EXTERNAL USE ONLY. DO NOT DRINK. Do not use on food surfaces or pets. Do not combine with other chemicals. |
DO NOT USE on children less than 6 months of age. |
When using this productkeep out of eyes, ears, mouth, and other body openings. In case of contact with eyes, rinse eyes thoroughly with water, remove contact lenses and continue rinsing eyes.
Stop use and ask a doctor if irritation or rash occurs. |
Keep out of reach of children. If swallowed get medical help or
contact a Poison Control Center right away. 1 (800) 222-1222
Directions:Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 9 years of age when using this product to avoid swallowing. |
Other information: Store between 10-30C (50-86F)
|
Inactive ingredients: Glycerin USP, fragrance, deionized water FDA REGISTERED NDC # 76915-1001-1 |
Lot # ####-##-## Recommended use-by date: MM/DD/YYYY
In this initial submission of this product listing, these label sections were renamed to the required label sections:
The above sections were originally submitted under other names, which caused the submission to fail validation
* Please review the disclaimer below.