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Drug Facts
Instant Hand Sanitizer
FDA Label NDC 76134-1111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Stericycle, Inc. for the product Instant Hand Sanitizer (NDC 76134-1111). 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 other, active ingredient, purpose, uses, warnings, otc - do not use, otc - stop use, 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 66.5%
Purpose
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 thoroughly 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
Stericycle, Inc.
Lake Forest, IL 60045
1-800-456-7077 option 3
www.stericycle.com
Reorder No. 17350SR
Principal Display Panel
NDC 76134-1111-0
Stericycle
Protecting People. Reducing Risk.
Instant
Hand
Sanitizer
Kills 99.9% of Germs
Enriched with
Aloe Vera
4 FL. OZ. (118 ML)
Principal Display Panel (Ste02 0000 01)
* Please review the disclaimer below.
