Bobbi Brown Extra
FDA Label NDC 64141-916

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 Bobbi Brown Extra (NDC 64141-916). 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, otc - when using, 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:  HOMOSALATE 10.00% [] OCTINOXATE 7.50% [] OXYBENZONE 5.00% [] AVOBENZONE 2.00%

Warnings

WARNING:  KEEP OUT OF EYES.  STOP USE IF IRRITATION OCCURS.

Otc - When Using

DIRECTIONS: WARM IN HANDS AND APPLY TO CLEAN SKIN

Package Label.Principal Display Panel

PRINCIPAL DISPLAY PANEL:


BOBBI BROWN

EXTRA

SPF 25 MOISTURIZING BALM

POIDS NET. 1.7 OZ / 50 ML


BOBBI BROWN PROFESSIONAL COSMETICS
NEW YORK, NY 10022
E109

WWW.BOBBIBROWN.COM

 



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