Active Ingredient
Ethyl alcohol 62%
Lucky
FDA Label NDC 20276-430
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Delta Brands, Inc for the product Lucky (NDC 20276-430). 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, when using this product, discontinue use, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
Sanitizing Hand Towel to help bacteria on the skin. Recommended for repeated use
Warnings
Flammable. Keep away from fire or flame.
For external use only
When Using This Product
avoid contact with eyes. In case of eye contact immediately flush eyes with water, call a doctor.
Avoid contact with broken skin.
Discontinue Use
if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor
Keep Out Of Reach Of Children
Children can only use this product with adult supervision. Do not drink. Not edible, in case of accidental ingestion seek professional assistance or contact a Poison Control Center immediately
Directions
Open the foil packet, unfold towel and wipe your hands. After use dispose properly. Do not flush down toilet
Inactive Ingredients
Water, Isopropyl Alcohol, Isopropyl Myristate, Propylene Glycol, Sodium Polyacrylate, Hydrogenated Polydecene, Trideceth-6, Fragrance, Glycerin, Polyquaternium-7, Tocopheryl Acetate, Methylchloroisothiazolinine, Methylisothiazolinone, Aloe Barbadensis Leaf Extract (Aloe Vera), Fragrance, Corn Oil
Package Label
Image Description (Luckywetwpesea)
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