Active Ingredient
TRICLOSAN 0.6 PERCENT
Antibacterial Foaming
FDA Label NDC 41250-185
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Meijer Distribution Inc for the product Antibacterial Foaming (NDC 41250-185). 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
ANTIBACTERIAL
Uses
HELPS REDUCE 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
IF IRRITATION AND 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 DRY HANDS, WORK INTO A LATHER VIGOROUSLY AND RINSE THOROUGHLY.
Inactive Ingredients
WATER, SODIUM LAURETH SULFATE, DIPROPYLENE GLYCOL, SODIUM XYLENESULFONATE, COCAMIDOPROPYL BETAINE, POLYSORBATE 20, FRAGRANCE, DISODIUM PHOSPHATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, RED 4 (CI 14700), YELLOW 5 (CI 19140).
Front And Back Labels
Image Of Label (Meijer1)
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