New Life Moisturizing Hand Sanitizer
FDA Label NDC 49681-100
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 New Life Moisturizing Hand Sanitizer (NDC 49681-100). 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, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethanol 70%
Purpose
Antiseptic
Indications & Usage
Uses • Hand sanitizer to decrease bacteria on skin • Recommended for repeated use
Warnings
Warning • For external use only
Flammable. Keep away from fire or flame.
When using this product avoid contact with face, eyes and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advice.
Stop use and ask doctor if irritation and redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Dosage & Administration
Directions • Wet hands thoroughly with product and rub into skin until dry. • Children under 6 years of age should be supervised by an adult when using this product.
Inactive Ingredient
Inactive Ingredients: Water (Aqua), Polysorbate 20, Isopropyl Alcohol, Tocopheryl Acetate, Panthenol, Methyl Gluceth-20, Acrylates/C10-30 Akyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum).
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