Otc - Active Ingredient
Active Ingredients
Ethyl Alcohol 70%
Spasoap
FDA Label NDC 71020-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sante Manufacturing Inc for the product Spasoap (NDC 71020-015). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, other safety information, instructions for use, otc - when using, 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 - Purpose
Purpose - Antiseptic
Indications & Usage
Use hand sanitizer to help reduce bacteria on the skin
Warnings
Warnings
Flammable
Other Safety Information
Keep away from fire or flame
Instructions For Use
For external use only
Otc - When Using
When using this product do not use in or near eyes. In case of contact, rinse eyes thoroughly with water
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away
Dosage & Administration
Directions
- apply palmful to hands
- rub hands together vigorously until dry
- supervise children in the use of this product
Inactive Ingredient
Water, Carbomer, Trethanolamine, Glycerin, Propylene Glycol, Alo Barbdensis Leaf Juice*, Tocopherol Acetate*, Lavandula Angustifolia Flower / Leaf / Stem Extract*, Fragrance*, D&C Red # 33*, FD&C Blue # 1*, FD&C Yellow # 5*,
* Contains 1 or more of these ingredients
Package Label.Principal Display Panel
​SpaSoap
Hand Sanitizer
2fl.oz (59ml) Each
6 fl.oz (177ml) Total
* Please review the disclaimer below.
