Otc - Active Ingredient
Alcohol
Duride Hand Sanitizer
FDA Label NDC 77498-210
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rainbow International Services Inc. for the product Duride Hand Sanitizer (NDC 77498-210). 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 otc - active ingredient, inactive ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Water(Aqua), Glycerin, Carbomer, Aloe Barbadensis Leaf Juice(Aloe Vera), Tocopheryl Acetate(Vitamin E), Phenoxyethanol, Aminomethyl propanol
Otc - Purpose
Antimicrobial
Indications & Usage
■ Hand sanitizer to help reduce bacteria on the skin.
Warnings
■ Flammable. Keep away from fire or flame.
■ For external use only.
Otc - Do Not Use
■ in children less than 2 months of age
■ on open skin wounds
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Storage And Handling
Store below 110℉(43℃)
Dosage & Administration
Pump 1-2 times and rub it into your hand. For topical use only.
* Please review the disclaimer below.
