Active Ingredient
TRICLOSAN 0.3 PERCENT
Antibacterial Foaming
FDA Label NDC 41520-171
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by American Sales Company for the product Antibacterial Foaming (NDC 41520-171). 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, stop using this product and ask 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
ANTISEPTIC
Uses
FOR WASHING TO DECREASE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ONLY.
When Using This Product
*AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.
Stop Using This Product And Ask Doctor If
* IRRITATION OR REDNESS DEVELOPS AND LASTS.
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Directions
PUMP ONTO WET HANDS, WORK INTO A LATHER. RINSE THOROUGHLY.
Other Information
STORE AT ROOM TEMPERATURE.
Inactive Ingredients
WATER (AQUA), SODIUM LAURETH SULFATE, GLYCERETH -26, DISODIUM LAURETH SULFOSUCCINATE, COCAMIDOPROPYL BETAINE, FRAGRANCE (PARFUM), PROPYLENE GLYCOL, PANTHENOL, ALOE BARBADENSIS LEAF JUICE, XANTHAN GUM, BENZOPHENONE-4, IMIDAZOLIDINYL UREA, DMDM HYDANTOIN, PEG-120 METHYL GLUCOSE DIOLEATE, PEG-7 GLYCERYL COCOATE, POLYSORBATE 20, TETRASODIUM EDTA, CITRIC ACID, RED 33 (CI 17200), BLUE 1 (CI 42090), YELLOW 5 (CI 19140)
Package Label.Principal Display Panel
Label Image (C1)
* Please review the disclaimer below.
