Active Ingredients
Ethyl Alcohol 70% v/v.................Antiseptic
Margaritaville
FDA Label NDC 72308-033
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Flex Beauty Labs for the product Margaritaville (NDC 72308-033). 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 ingredients, purpose, use, safety instructions, when using this product, do not use, 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
hand sanitizer to help reduce bacteria on the skin
Safety Instructions
Flammable, Keep away from fire and flame
When Using This Product
In case of contact,rinse eyes thoroughly with water
Do Not Use
Do not use in or near eyes.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact Poison Control center right away.
Directions
- apply palmful to hands.
- rub hands together vigorously until dry.
- supervise children in the use of this product.
Other Information
Store below 110°F (43°C)
May discolor certain fabrics or surfaces.
Inactive Ingredients
Water, Carbomer, Triethanolamine, Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance, Yellow 5 (CI19140), Red 33
Package Label.Principal Display Panel
1 (1)
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