Active Ingredient
Alcohol Denat. 62%
Hand Sanitizer
FDA Label NDC 76383-014
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bbc Group Limited for the product Hand Sanitizer (NDC 76383-014). 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, when using this product, 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
Antiseptic
Uses
■ to decrease bacteria on the skin that could cause disease ■ recommended for repeated use
Warnings
For external use only. Flammable, keep away from fire or flame
When Using This Product
■ keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ avoid contact with broken skin ■ do not inhale or ingest
Stop Use And Ask A Doctor If
■ irritation and redness develop ■ condition persists for more than 72 hours
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 ■ for children under 6, use only under adult supervision ■ not recommended for infants
Other Information
■ do not store above 105°F ■ may discolor some fabrics ■ harmful to wood finishes and plastics
Inactive Ingredients
Water, PEG-40 Hydrogenated Castor Oil, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide, Denatonium Benzoate, Tocopheryl Acetate
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