Active Ingredient
Ethyl Alcohol 70% v/v
Summit 375 Gel Alcohol Hand Sanitizer Gel
FDA Label NDC 23590-400
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by R.l. Williams Company for the product Summit 375 Gel Alcohol Hand Sanitizer (NDC 23590-400). 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 - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin Sanitizer
Uses
- Hand sanitizer to help reduce bacteria on the skin
- Recommended for repeated use
Warnings
Flammable, keep away from fire or flame.
For external use only.
When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately.
Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.
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.
Directions
- Dispense an adequate amount in your palm to cover all surface of hands completely.
- Rub hands together until dry.
- Supervise children in the use of this product.
Other Information
- Do not store above 100 °F (38 °C)
- May discolor some fabrics
Inactive Ingredients
Water, Glycerin, Carbomer, Propylene Glycol, Diisopropylamine, Fragrance
Package Label.Principal Display Panel
Product Label (850 mL Cartridge (Front))
Product Label (850 mL Cartridge (Back))
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