Otc - Active Ingredient
Alcohol
Maum Hand Sanitizer Gel
FDA Label NDC 71909-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cnt Dream. Co., Ltd for the product Maum Hand Sanitizer Gel (NDC 71909-0002). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, 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, etc
Otc - Purpose
Antiseptic
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry.
Supervise children in the use of this product.
Warnings
For external use only.
Flammable.
Keep away from fire or flame.
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Label)
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