Active Ingredient(S)
Benzalkonium Chloride 0.1%. Purpose: Antiseptic
Antibacterial Hand Sanitizer
FDA Label NDC 74621-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aogrand International Trade Corporation for the product Antibacterial Hand Sanitizer (NDC 74621-006). 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(s), purpose, use, warnings, otc - do not use, when using this product, stop use and ask a doctor, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
- hand Sannitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
- recommended for repeated use
Warnings
For external use only.
Otc - Do Not Use
Do not apply around eyes. Do not use in ears & mouth.
When Using This Product
avoid contact with eyes. In case of contact, flush eyes with water.
Stop Use And Ask A Doctor
if redness or irritation develop and persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be supervised in use of this product.
Directions
- Place enough product into your palms and thoroughly spread on both hands
- rub into skin until dry
Inactive Ingredients
Cocamidopropylamine oxide, C12-20 Alkyl glycoside, glycerin, hydroxyethyl cellulose, Casone (methylisothiazolinone and methylchloroisothiazolinone), citric acid, deionized water
Other Information
- store below 110F (43C)
- may discolor certain fabrics or surfaces
Package Label - Principal Display Panel
480g NDC: 74621-006-02
Pdp (74621 006 02)
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