Active Ingredient
TRICLOSAN 0.115%
Renewal
FDA Label NDC 11822-2108
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid for the product Renewal (NDC 11822-2108). 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
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
APPLY ONTO WET HANDS. WORK INTO A LATHER, RINSE THOROUGHLY.
Questions Or Comments
1-866-695-3030
Other Information
STORE AT ROOM TEMPERATURE.
Inactive Ingredients
WATER, SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, DECYL GLUCOSIDE, SODIUM CHLORIDE, FRAGRANCE, DMDM HYDANTOIN, PEG-120 METHYL GLUCOSE DIOLEATE, CITRIC ACID, TETRASODIUM EDTA, POLYQUATERNIUM-7, PEG- 7 GLYCERYL COCOATE, RED 33 (CI 17200), BLUE 1 (CI 42090).
Package Label.Principal Display Panel
Image Of Renewal Liquid Hsoap (Raabs80)
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