Otc - Active Ingredient
Active Ingredient Purpose
Ethyl Alcohol 62% w/w Antiseptic
Instant Hand Sanitizer
FDA Label NDC 25225-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Unique Holding Group Inc for the product Instant Hand Sanitizer (NDC 25225-015). 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, description, warnings, indications & usage, storage and handling, inactive ingredient, 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
Description
Uses:
Hand sanitizer to help decrease bacteria on the skin that could cause diseases
Warnings
Warnings:
Flammable. Keep away from fore or flame.
For external use only-hands.
When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a physician if irritation or skin rash develops.
Keep out of reach of children
if accidentally ingested, seek medical help or contact a Poison Control Center immediately.
Indications & Usage
Directions
- Place enough product in your palm to thoroughly cover your hands
- rub hands briskly together until dry
- children under 6 years of age should be supervised when using this product
Storage And Handling
Other Information
- Store below 105F
- May discolor certain fabrics.
- Maybe harmful to wood finishes and plastics
Inactive Ingredient
Inactive Ingredients:
carbomer, fragrance, glycerin, triethanolamine, propylene glycol, deionized water, aloe barbadensis gel
Package Label.Principal Display Panel
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Bottle Label (Bottle)
card
Blister Card (Card)
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