Active Ingredient
Benzethonium chloride, 0.2% w/v
Dermatize
FDA Label NDC 63131-0004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Anderson Chemical Company for the product Dermatize (NDC 63131-0004). 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, use, warning, when using this product, 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
Antiseptic
Use
For handwashing to decrease bacteria on skin.
Warning
For external use only.
When Using This Product
- discontinue use if irritatio and redness develop.
- do not use in or near eyes.
Stop Use And Ask A Doctor If
Stop use and ask a doctor if irritation or redness develops, or if conditions persist for more than 72 hours.
Keep Out Of Reach Of Children.
Keep out of reach of children, except under adult supervision.
- In case of accidental ingestion, see medical attention or contact a poision control cernter immediately.
Directions
- Hands need not be washed prior to using.
- For one step hand wash/antiseptic skin cleaning.
- Place 5 milliliters in palm of hand, add water, work up a lather and scrub for 30 seconds.
- Rinse hands thoroughly with potable water after washing.
Inactive Ingredients
Citric acid; 1,3-Dihydroxymethyl-5,5-dimethylhydantoin and 3-iodo-2-propynyl butyl carbamate; Ethoxylated C11 Alcohol; Hydrogenated starch hydrolysate; Hydroxypropyl methylcellulose; N-alkykl (C12-C16)-N, N-dimethylamine oxide; Sodium hydroxide; Water.
Questions Or Comments?
320-693-2477
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Product Label (Dermatize)
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