Active Ingredient
Active Ingredient
Benzalkonium Chloride .13%
Sanitaxe Antibacterial Gel
FDA Label NDC 72197-033
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by American Consumer Products Corp for the product Sanitaxe Antibacterial (NDC 72197-033). 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
Purpose
Antiseptic
Uses
Uses ● Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
Warnings – For external use only. Do not ingest or swallow.
Do not apply around eyes. Do not use in ears & mouth.
When Using This Product
When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
Stop Use And Ask A Doctor
Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.
Keep Out Of Reach Of Children
Keep out of reach of children. Do not use on children less than 2 months of age.
Supervise use in children under 6 years of age to prevent accidental swallowing.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions ● Pump onto wet hands ● Work into lather ● Wash hands, rinse and dry thoroughly.
Inactive Ingredients
Inactive ingredients: Water (Aqua), Cocamidopropyl Betaine, Sodium Cocoamphoacetate, PEG-150 Disterate, Fragrance, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Yellow No. 5, D&C Red No. 33.
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