Active Ingredient
Ethyl Alcohol 66.5%
Aramark Hand Sanitizer
FDA Label NDC 81238-1112
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Western First Aid Safety Dba Aramark for the product Aramark Hand Sanitizer (NDC 81238-1112). 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, purpose, uses, warnings, do not use in eyes., stop use and ask a doctor if, 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
Purpose
Antibacterial
Uses
■ for hand washing to decrease bacteria on skin without soap and water
■ recommended for repeated use
Warnings
For external use only.
Flammable., keep away from fire or flame.
Do Not Use In Eyes.
If this happens, rinse eyes thoroughly with water.
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 and wrists thoroughly with product and allow to dry without wiping
■ children under 6 years of age should be supervised while using this product
Inactive Ingredients
aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified
water, triethanolamine
Package Labeling
aramark
25 ct. Each Packet Net. Wt. 0.9g
HAND SANITIZER
Kills 99.9% of Germs
Enriched with Aloe Vera
NDC 81238-1112-2
aramarkuniform.com
MANUFACTURED FOR:
Aramark
Lenexa, KS 66219
(913) 269-9611
Please retain carton for drug information.
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