Bodycology
FDA Label NDC 51345-065
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Advanced Beauty Systems, Inc. for the product Bodycology (NDC 51345-065). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, 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
Otc - Purpose
Uses To decrease bacteria on the skin.
Otc - Keep Out Of Reach Of Children
Indications & Usage
Stop use and consult doctorif irritation and redness develop and persist for more than 72 hours.
Warnings
Warnings
For external use only.
FLAMMABLE. Keep away from heat and flame.
When using this product
-Avoid contact with eyes. If contact occurs, flush eyes with water.
-Avoid contact with broken skin.
Dosage & Administration
Inactive Ingredient
Inactive ingredients: Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI 77007).
May Contain: FD&C Red No. 4 (CI 14700), FD&C Yellow No. 5 (CI 19140), FD&C Blue No. 1 (CI 42090), D&C Red No. 33 (CI 17200).
Package Label.Principal Display Panel
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