Dosage & Administration
Store between 15-30°C (59-86°F),Avoid freezing and excessive heat aboe 40°C (140°F).
Hand Sanitizer
FDA Label NDC 55866-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Keman Technology Co., Ltd. for the product Hand Sanitizer (NDC 55866-004). 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 dosage & administration, inactive ingredient, indications & usage, otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Water，Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Ammonium Hydroxide
Indications & Usage
1.Place enough product on hands to cover all surfaces. Rub hands together until dry.
2.Supervise children under 6 years of age when using this produc to avoid swallowing.
Otc - Active Ingredient
Ethanol
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
Warnings
For external use only. Flammable. Keep away from heat or flame.
Package Label.Principal Display Panel
Label (Label)
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