Active Ingredient
Ethyl Alcohol
Dews Plus
FDA Label NDC 73824-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dp Import & Export, Inc. for the product Dews Plus (NDC 73824-001). 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, keep out of reach of children., directions, other informatin, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
- Hand sanitizer to help decrease bacteria on the skin.
- When water, soap towel are not available
- Recommended for repeated use.
Warnings
External use only.
Flammable, Keep away from fire or flame
Do not use
- In children less than 2 months of age
- On open skin wounds
When using this product, avoid contact with eyes
in case of contact flush eyes with water.
Stop use and ask a doctor if redness or irritation
develop and persist for more than 72hours.
Keep Out Of Reach Of Children.
Children must be supervised in use of this product.
Supervise children under 6 years of age when using this
product to avoid swallowing.
Directions
Place enough product on hands to cover all surfaces, Rub hands together until dry
Other Informatin
Store at15°30°c(59"to86F)
Avoid freezing and excessive heat above 40C(104%F)
Inactive Ingredient
water, triethanolamine
glycerin, propylene glycol, Vitamin E, aloe vera gel
carbomer
Product Label
Image Description (60ml)
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