Active Ingredient
Benzalkonium Chloride (0.13%)
Up And Up Liquid
FDA Label NDC 82442-088
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 Inc. for the product Up And Up (NDC 82442-088). 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 use and ask a doctor, 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 hand washing to decrease bacteria on the skin.
Warnings
For external use only
When Using This Product
- Avoid contact with eyes. In case of contact, flush with water.
Stop Use And Ask A Doctor
if irritation or redness develops and lasts for more than 72 hours.
Keep Out Of Reach Of Children.
if swallowed, get medical help or contact a Poison Control center right away.
Directions
- Apply onto dry hands.
- Lather and rinse thoroughly with water.
Inactive Ingredients.
Water (Aqua), Cocamidopropyl Betaine, Hydroxyethylcellulose, Tetrasodium EDTA, Glycerin, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Poloxamer 124, Fragrance (Parfum), Red 40 (CI 16035), Yellow 5 (CI 19140), Red 33 (CI 17200).
Questions
1-800-910-6874
Principal Display Panel
Principal Display Panel (Pdp)
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