Active Ingredients
Ethyl Alcohol 62%
Hand Sanitizer Gel
FDA Label NDC 84641-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nantong Qinji Health Technology Co., Ltd. for the product Hand Sanitizer (NDC 84641-006). 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 ingredients, purpose, use, warnings, when using this produce,, discontinue use if, keep out of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
For hand sanitizing to reduce bacteria on the skin
Warnings
For external use only. Flammable.
Keep away from fire or flame.
When Using This Produce,
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Discontinue Use If
irritation or redness develops
Keep Out Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Squeeze small amount in your palm and briskly rub hands together until dry.
Inactive Ingredients
Water, Glycerin, Carbomer, Fragrance, Triethanolamine, Aloe Barbadensis Leaf Juice, Vitamin E, Iron Oxide (CI 77499), Iron Oxide (CI 77492), D&C Red No.30.
84641-006-01
84641-006-01 (84641 006 01)
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