Otc - Active Ingredient
Alcohol (Ethanol)
Germfree Hand Sanitizer Babypowder Fragrance
FDA Label NDC 70812-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biostech Co., Ltd. for the product Germfree Hand Sanitizer Babypowder Fragrance (NDC 70812-002). 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 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
Glycerin, Triethanolamine, Carbomer, Fragrance, Water
Otc - Purpose
Antiseptic
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
do not use in or near the eyes. If contact occurs, rinse thoroughly with water.
avoid contact with broken skin.
Warnings
For external use only.
Flammable, keep away from heat and flame.
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.
Dosage & Administration
wet hands thoroughly with product briskly rub hands together until dry supervise children under 6 years in the use of this product
Package Label.Principal Display Panel
Label (Label)
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