Dosage & Administration
Keep in dry and cool places, away from fire.
Instant Hand Sanitizer
FDA Label NDC 52923-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Adf Hi-tech Disinfectants Co., Ltd. for the product Instant Hand Sanitizer (NDC 52923-002). 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
carbomer，glycerine，purified water
Indications & Usage
Put proper amount of the product on palm and rub thoroughly until dry.
Otc - Active Ingredient
Ethanol
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
No Rinseing
Warnings
Flammable. For external use only. Avoid contact with eyes and broken skin. Discontinue use if irritation develops.
Package Label.Principal Display Panel
Label (Label)
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