Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 65%
Bodycology
FDA Label NDC 51706-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Landy International for the product Bodycology (NDC 51706-201). 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, warnings, indications & usage, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
Warnings: For external use only. When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Indications & Usage
Uses: to decrease bacteria on the skin that could cause disease
Directions: wet hands, apply palmful to hands, scrub thoroughly for 30 seconds, rinse.
Inactive Ingredient
Inactive Ingredients: Water (Aqua), Isopropyl Myristate, Propylene Glycol, Triethanolamine, Carbomer, Fragrance (Parfum), Aloe Barbadensis (Aloe Vera) Leaf Juice, Yellow 5 (CI 19140), Ext. Violet 2 (CI 60730)
Image Of Back Label.jpg (Back)
Package Label.Principal Display Panel
Cherry Blossom Hand Sanitizer
30 mL 1 FL OZ
Image Of Front Label (Front)
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