Drug Facts
Active Ingredients
Triclosan 0.115%
Triclosan
FDA Label NDC 50157-119
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brands International for the product Triclosan (NDC 50157-119). 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, purpose, uses, warnings, stop use and ask a doctor if, when using this product, 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
Uses
for handwashing or decrease bacteria to the skin
Warnings
For external use only
Stop Use And Ask A Doctor If
irritation or redness develops
When Using This Product
- do not get it into eyes, if contact occurs, rinse eye thoroughly with water
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
- Wet hands
- apply palmful to hands
- scrub throughly
- rinse
Inactive Ingredients
Water, Sodium Laureth Sulfate, Sodium Chloride, DMDM Hydantoin, Citric Acid, Fragrance, EDTA, Yellow #5, Red# 33
Package Label
Spa Soap
Antibacterial
Liquid Soap
Refill
* Please review the disclaimer below.
