Active Ingredient(S)
Ethyl Alcohol 75% v/v
Al Kogel Hand Sanitizer
FDA Label NDC 52989-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Taizhou Yadai Daily-use Co., Ltd. for the product Al Kogel Hand Sanitizer (NDC 52989-006). 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 - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand sanitizer to help decrease bacteria on the skin
Recommended for repeated use
Warnings
For external use only. Flammable. Keep away from fire or flame
When using this product, do not use in or near eyes
Stop use and ask a doctor if redness or irritation develop and last for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.
Directions
- Pump as needed into your palms and thoroughly spead on both hands. Rub into skin until dry.
Other Information
Store at room temperature no higher than 45 C (113 F) and under shade. Keep in closed containers and free from direct sunlight.
Inactive Ingredients
Carbomer, Triethanolamine, Glycerin, Water
* Please review the disclaimer below.
