Brightening Powder
FDA Label NDC 64141-718

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bobbi Brown Professional Cosmetics Inc. for the product Brightening Powder (NDC 64141-718). 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, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

ACTIVE INGREDIENTS: TITANIUM DIOXIDE 18.60% [] OCTINOXATE 7.00% [] ZINC OXIDE 5.80%

Package Label.Principal Display Panel

PRINCIPAL DISPLAY PANEL:

BOBBI BROWN

BRIGHTENING POWDER COMPACT FOUNDATION

SPF 20

REFILL/RECHARGE

NT WT. .38 OZ/ 11 g



DISTR. BOBBI BROWN PROFESSIONAL COSMETICS

NY, NY 10022

E3L7

BOBBI BROWN.COM







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