Active Ingredient(S)
Ethyl Alcohol 62%. Purpose: Antiseptic
Antibacterial Hand Sanitizer
FDA Label NDC 77165-350
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Klm Promo Products, Llc for the product Antibacterial Hand Sanitizer (NDC 77165-350). 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, do not use, otc - when using, otc - stop use, 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
Decrease bacteria and germs on the hands
when water, soap, and towel are not available
recommended for repeated use
Warnings
For external use only.
Do Not Use
Do not use in ears and mouth
Otc - When Using
When using this product avoid contact with eyes. In case of contact flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops or persists.
Otc - Keep Out Of Reach Of Children
Children under 6, use only under adult supervision. Not recommended for infants.
Directions
- pump as needed on to your palms and thoroughly spread on both hands
- rub into skin until dry
Other Information
- store at 20℃(68℉-77℉)
- may discolor fabrics
- do not leave under high heat
Inactive Ingredients
Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Fragrance, Disodium EDTA , Tocopheryl Acetate, Deionized Water
Package Label - Principal Display Panel
30 mL NDC: 77165-350-01
antibacterial hand sanitizer
1 fl.oz. (30ml)
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