Derma-glove
FDA Label NDC 24673-249
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rwm Technologies for the product Derma-glove (NDC 24673-249). 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 description, otc - active ingredient, otc - purpose, indications & usage, warnings and precautions, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active Ingredient
Ethanol 60%..................................................................Antibacterial
Triclosan 0.3% ..............................................................Antiseptic
Otc - Purpose
Antiseptic/Antimicrobial hand sanitizer spray
Indications & Usage
- Hand sanitizer to help reduce bacteria on the skin that could cause disease
- Recommended for repeated use
Warnings And Precautions
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Otc - When Using
When using this product do not use in or near eyes. In case of eye contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if skin irritation or redness develops and persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Dosage & Administration
- Spray enough product in your palm to thoroughly cover your hands
- Rub hands together briskly until dry
- Rinse with water after use
- Children under 6 years of age should be supervised when using this product
General Precautions
- Do not store above 110o F (43o C)
- For additional information, see Material Safety Data Sheet (MSDS).
Inactive Ingredient
Otc - Questions
Questions or Comments?
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