Active Ingredient
Chloroxylenol 0.3%
Lucky
FDA Label NDC 20276-151
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 20276-151). 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, use, warnings, when using this product, stop use and ask a doctor if, 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
Antibacterial
Use
for handwashing to decrease bacteria on the skin
Warnings
For external use only
When Using This Product
■ avoid contact with the eyes. In case of eye contact, flush with water.
Stop Use And Ask A Doctor If
■ irritation and redness develops
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
■ pump into hands, wet as needed ■ lather vigorously for at least 15 seconds ■ wash skin, rinse thoroughly and dry
Inactive Ingredients
water (aqua), ammonium lauryl sulfate, cocamidopropyl betaine, ammonium chloride, DMDM hydantoin, fragrance, citric acid, tetrasodium EDTA, FD&C yellow no. 5, FD&C red no. 40
Package Label
Package Label (Abliqudsoapregchlrxylnl)
* Please review the disclaimer below.
