Active Ingredient
TRICLOSAN 0.15%
Equaline
FDA Label NDC 41163-220
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Supervalu Inc for the product Equaline (NDC 41163-220). 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, otc - when using, stop use 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
FOR WASHING TO DECREASE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ONLY.
Otc - When Using
WHEN USING THIS PRODUCT AVOID CONTACT WITH THE EYES. IF CONTACT OCCURS, RINSE EYES THROUGHLY WITH WATER.
Stop Use 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
SQUEEZE ONTO WET HANDS, WORK INTO A LATHER AND RINSE THOROUGHLY.
Other Information
STORE AT ROOM TEMPERATURE
Inactive Ingredients
WATER, SODIUM LAURETH SULFATE, AMMONIUM LAURYL SULFATE, DECYL GLUCOSIDE, COCAMIDOPROPYL BETAINE, GLYCERIN, SODIUM CHLORIDE, PEG-18 GLYCERYL OLEATE/COCOATE, FRAGRANCE , COCAMIDE MEA, DMDM HYDANTOIN, TETRASODIUM EDTA, CITRIC ACID,YELLOW 5 (CI 19140), RED 4 (CI 14700).
Package Label.Principal Display Panel
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