Otc - Active Ingredient
Active ingredient
Triclosan 0.2%
Lucky
FDA Label NDC 20276-050
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 20276-050). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antibacterial
Indications & Usage
Uses • for hand washing to decrease bacteria on the skin.
Warnings
Warnings • For external use only
Otc - When Using
When using this product • avoid contact with eyes • in case of eye contact, flush with water.
Otc - Stop Use
If irritation and redness develops, stop use and ask a doctor
Otc - Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control Center right away. Keep out of the reach of children.
Dosage & Administration
Directions •wet bar with water • lather vigorously and wash skin • rinse and dry thoroughly.
Inactive Ingredient
Inactive ingredients sodium palm kernelate, sodium palmate, water, fragrance, glycerin, sodium chloride, tetrasodium EDTA, titanium dioxide, FDC yellow no. 5, FDC yellow no. 6
Package Label.Principal Display Panel
Image Of Package Label (Antbcbrsplcky)
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