Otc - Active Ingredient
Active Ingredient
Hydroquinone 2%
Body Fade Creme
FDA Label NDC 59735-304
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biocosmetic Reasearch Labs for the product Body Fade Creme (NDC 59735-304). 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, otc - do not use, otc - stop use, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Skin Lightener Cream
Indications & Usage
Uses
For gradual fading of dark (brownish) spots.
Warnings
Warnings
Avoid contact with eyes.
Otc - Do Not Use
Do not use on children under 12 years of age.
Otc - Stop Use
Some users may experience a mild irritation. If skin Irritation becomes severe, stop use and consult a doctor.
Dosage & Administration
Directions
Apply all over your body twice daily. Pay special attention to problem areas like knees and elbows.
Inactive Ingredient
Inactive Ingredients
Water (Aqua), Isopropyl Palmitate, Stearic Acid, Propylene Glycol, Cetyl Alcohol, DEA-Cetyl Phosphate, glycerin, Dimethicone, Tocopheryl Acetate, Sodium PCA, Aloe Barbadensis Leaf Extract, Citrus Unshiu Peel Extract, Sodium Palmitoyl Proline, Nymphaea Alba Flower Extract, Polyacrylamide, Hydroxyethylcellulose, Fragrance, C13-14 Isoparaffin, Laureth-7, EDTA, Sodium Sulfite, Sodium Metabisulfite, Diazolidinyl Urea, Iodopropynyl Butylcarbamate, Blue 1 (CI 42090), Yellow 5 (CI 19140)
Package Label.Principal Display Panel
Image Of Carton (Bodyfademax1)
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