Active Ingredient
TRICLOSAN 0.115%
Le Techniq
FDA Label NDC 42507-719
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hyvee Inc for the product Le Techniq (NDC 42507-719). 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 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
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 A Doctor If
IRRITATION OR REDNESS DEVELOP
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, SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, DECYL GLUCOSIDE, FRAGRANCE, DMDM HYDANTOIN, SODIUM CHLORIDE, PEG-120 METHYL GLUCOSE DIOLEATE, TETRASODIUM EDTA, SODIUM SULFATE, POLYQUATERNIUM-7, CITRIC ACID, POLOXAMER 124, PEG-7 GLYCERYL COCOATE, D&C RED 33 (CI 17200), FD&C BLUE 1 (CI 42090)
Label Copy
Image Of The Labe (13630l)
* Please review the disclaimer below.
