Active Ingredient
BENZALKONIUM CHLORIDE 0.13%
Up And Up
FDA Label NDC 11673-815
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Up And Up (NDC 11673-815). 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
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 THOROUGHLY WITH WATER
Stop Using This Product And Ask Doctor If
IRRITATION AND REDNESS DEVELOPS
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY
Directions
SQUEEZE A SMALL AMOUNT ONTO A WET WASHCLOTH, SPONGE, POUF OR HANDS AND APPLY TO BODY. WORK INTO A RICH LATHER AND RINSE OFF
Other Information
STORE AT ROOM TEMPERATURE
Inactive Ingredients
WATER (AQUA), COCAMIDOPROPYL BETAINE, DECYL GLUCOSIDE, HYDROXYETHYLCELLULOSE, GLYCERIN, CITRIC ACID, POLOXAMER 124, FRAGRANCE (PARFUM), TETRASODIUM EDTA, POLYQUATERNIUM-7, SODIUM CITRATE, ALOE BARBADENSIS LEAF JUICE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, BLUE 1 (CI 42090), EXT. VIOLET 2 (CI 60730)
Questions Or Comments?
1-800-910-6874
Label Copy
Image Of The Label (19528l)
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