Active Ingredient
Benzalkonium Chloride 0.3%
Alcohol Free Hand Sanitizer Gel
FDA Label NDC 87001-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Haian Kangrui Textile Co., Ltd. for the product Alcohol Free Hand Sanitizer (NDC 87001-004). 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，, discontinue use, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For hand sanitizing to reduce bacteria on the skin.
Warnings
For external use only.
Flammable. Keep away from fire and flame.
When Using This Product，
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 Reach 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, POLYOXYL 40 HYDROGENATED CASTOR OIL, HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%), GLYCERIN, PHENOXYETHANOL, FRAGRANCE.
87001-004-01
87001-004-01 (87001 004 01)
87001-004-02
87001-004-02 (87001 004 02)
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