Active Ingredient
Alcohol 70% v/v
The following Structured Product Label (SPL) was submitted to the FDA by Zep Inc. for the product Zep Fuzion Instant Hand Sanitizer (NDC 66949-119). 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, do not use, when using this product, stop use and ask doctor, keep out of reach of children and pets, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Alcohol 70% v/v
Antiseptic
■ To help reduce germs and bacteria on the skin.
■ Recommended for repeated use.
■ No rinsing required.
Flammable. Keep away from fire, flame, or spark. For external use only.
in the eye; if in eyes, rinse thoroughly with water.
■ Do not swallow.
■ If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.
Stop use and ask doctor if skin irritation or redness persists for more than 72 hours.
Keep out of reach of children and pets. Children must be supervised in use of this product.
■ Keep container closed and stored in a dry area at temperatures between 68°F and 77°F (20°C and 25°C).
■ Do not reuse empty container.
■ Dispose in accordance with all applicable federal, state and local regulations
Deionized Water, PEG-6 (and) Acrylates/Vinyl Crosspolymer, Fragrance.
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