Otc - Active Ingredient
Alcohol 70% Purpose Antiseptic
Prosanca
FDA Label NDC 77838-236
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Proem Group for the product Prosanca (NDC 77838-236). 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, warnings, indications & usage, otc - keep out of reach of children, dosage & administration, otc - purpose, 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, Glycerin, Hydrogen peroxide
Warnings
For external use only, Flammable, Keep away from heat or flam.
Do not use: in children less 2 months of age on open skin wounds
When use this product: this product keep out of eyes,ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs, these may be signs of s serious condition
Keep out of reach of children. If swallow get medical or contact of poison Control Center right away
Indications & Usage
Hand Sanitizer to help reduce bateria that potentially can cause disease for use when soap are not available
Otc - Keep Out Of Reach Of Children
If swallow, get medical help or contact o poison control Center right away.
Dosage & Administration
70% Ethanol alcohol
Otc - Purpose
Use Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap are not avalble.
Package Label.Principal Display Panel
3.8L/128 fl-oz ( 1 GAL) NDC: 77838-668-05
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