Active Ingredient
Alcohol 75% v/v
Hand Sanitizer
FDA Label NDC 76383-058
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 76383-058). 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, use, warnings, do not use, when using this product, stop use and ask a doctor if, 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
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria on skin
Warnings
For external use only. Flammable. Keep away from flame or heat.
Do Not Use
■ On children less than 2 months of age ■ On open skin wounds
When Using This Product
■ Do not use in or near eyes. ■ In case of contact, immediately rinse eyes throughly with water.
Stop Use And Ask A Doctor If
Irritation or rash appears ■ conditions persist for more than 72 hours ■ if redness is present
Keep Out Of Reach Of Children
If accident or swallowed, contact a doctor or poison control center immediately.
Directions
■ Apply a dime sized amount to hands. Rub hands together until dry ■ Supervise children under 6 years of age when using this product to avoid swallowing
Other Information
Store between 15°-30°C (59-86°F). ■ May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Aloe Barbadensis leaf juice, Glycerin, Tocopheryl Acetate (Vitamin E), Triethanolamine, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer
Questions
Tel: 332-210-9092 (Mon-Fri 9am-5pm EST)
Package Label
Package Label (Hndsntzrgel75gel)
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