OTC Medication Information: Ili Hand Sanitizer Instant

ILI HAND SANITIZER INSTANT- alcohol gel
Strong Brands, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active Ingredient: Ethyl Alcohol 63%

Purpose: Antiseptic

Use: For hand washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings: Flammable, keep away from fire or flame. For external use only. 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. If condition persists for more than 72 hours consult a doctor.

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 and allow to dry without wiping.

Questions? 1-323-284-9021 weekdays, 9am to 5pm PST

ili Hand Sanitizer 8 fl oz

8 fl oz Ili Hand Sanitizer Label
(click image for full-size original)

water, isopropyl alcohol, glycerin, methyl gluceth-20, panthenol, tocopheryl acetate, benzalkonium chloride, polysorbate 20, carbomer, sodium benzotriazolyl butylphenol sulfonate, aminomethyl propanol, fragrance

ILI HAND SANITIZER INSTANT
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:50859-100
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Alcohol (Alcohol) Alcohol 63 mL in 100 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50859-100-01 236.6 mL in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 06/01/2010
Labeler — Strong Brands, Inc. (962050543)

Revised: 06/2010 Strong Brands, Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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