Active Ingredient
Ethyl Alcohol 66.5%
Instant Hand Sanitizer
FDA Label NDC 49959-1111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Graphic Controls for the product Instant Hand Sanitizer (NDC 49959-1111). 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 active ingredient, pupose, uses, warnings, otc - do not use, otc - stop use, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Pupose
Antiseptic
Uses
- for handwashing to decrease bacteria on skin
- recommended for repeated use
Warnings
For external use only. Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use in the eyes. If this happens, rinse thoroughly with water
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours
Keep Out Of Reach Of Children
If ingested get medical help or contact a Poison Control Center right away
Directions
- wet hands thorough with product
- allow to dry without wiping
- children under 6 should be supervised while using this product
Inactive Ingredients
aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine
Manufactured for Graphic Controls LLC
Buffalo, NY 14204
1-800-669-1535
Package Label - Principal Display Panel – Bottle
FREE Sample-Not for Resale
GRAPHIC CONTROLS LLC – Instant Hand Sanitizer
For more information or To Order call
800-665-1535
www.graphiccontrols.com
Kills 99.99% of Germs
Enriched with Aloe Vera
Package Label (PRINCIPAL DISPLAY PANEL – BOTTLE)
* Please review the disclaimer below.
