Dosage & Administration
Store below 110°F (43°C).
Hand Sanitizer
FDA Label NDC 55866-005
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 55866-005). 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
Put enough product in your palm to cover hands and rub hands together briskly until dry.
Otc - Active Ingredient
Ethanol
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
Warnings
Flammable. Keep away from fire or flame. For extermal use only When using this product, do not use in or near the eyes. In case of contact, rinse eyes throughly with water. Stop use and ask a doctor if iritation or rash appears and lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Package Label.Principal Display Panel
Label (Label)
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