Active Ingredient
Ethyl Alcohol 66.5%(v/v)
Be Smart Get Prepared Hand Sanitizer Gel
FDA Label NDC 55550-106
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Total Resources International, Inc for the product Be Smart Get Prepared Hand Sanitizer (NDC 55550-106). 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, otc - do not use, otc - stop use, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For handwashing to decrease bacteria on skin without soap and water.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use in eyes, if this happens, rinse thoroughly with water.
Otc - Stop Use
Stop use, ask a doctor if irritation develops and persists for 72 hours.
If ingested, get medical help or contact a Poison Control Center right away.
Directions
- wet hands & wrists thoroughly with product and allow to dry without wiping
Inactive Ingredients
aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine
Principal Display Panel – 1 Ml Pouch Label
BE SMART
GET PREPARED®
HAND SANITIZER
0.05 oz [1.50 g]
Kills 99.9% of Germs
Aloe Vera • Single Use
Made in USA
Manufactured for Total Resources Intl. Inc
Walnut, California 91789
www.trikits.com • 00-SAN-9600 Rev.01
NDC 55550-106-02
Principal Display Panel – 1 mL Pouch Label (Bex01 0000 01)
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