Instant Hand Sanitizer - Original
FDA Label NDC 10586-9103
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Core Brands, Inc. for the product Instant Hand Sanitizer - Original (NDC 10586-9103). 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 drug facts, active ingredient, purpose, uses, warnings, do not use, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 62%
Purpose
Antimicrobial
Uses
- for handwashing to decrease bacteria on the skin
- recommended for repeated use
Warnings
For external use only.
Flammable, keep away from fire or 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.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- wet hands thoroughly with product
- briskly rub hands together until dry
- supervise children in the use of this product
Other Information
- store at 20 degrees to 25 degrees C (68 degrees to 77 degrees F)
- may discolor certain fabrics
Inactive Ingredients:
aloe vera leaf juice, carbomer, fragrance, glycerin, propylene glycol, tocpheryl acetate, triethanolamine, water.
Distributed By: Greenbrier International, Inc. Chesapeake, Va 23320 Made In China
Instant Hand Sanitizer Extra Enriched With Vitamin E Bead Original Label (10586-9103-8)
Originallabel (Originallabel)
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