Lusti Skin Softening Hand Sanitizer
FDA Label NDC 49681-400
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by New Life Products, Inc. for the product Lusti Skin Softening Hand Sanitizer (NDC 49681-400). 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 drug facts, active ingredient, purpose, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 65%
Purpose
Antiseptic
Inactive Ingredients
Water (Aqua), Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Mentha Piperita (Peppermint) Oil, Panthenol, Tocopheryl Acetate, Fragrance(Parfum).
Packaging
Image (Lusti)
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