Otc - Active Ingredient
ACTIVE INGREDIENTS: HOMOSALATE 5.00% [] OCTISALATE 5.00% [] AVOBENZONE 3.00% [] OXYBENZONE 3.00%
Bobbi Brown Brightening Protective Face Base
FDA Label NDC 64141-005
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 Brightening Protective Face Base (NDC 64141-005). 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 - when using, warnings, 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 - When Using
DIRECTIONS: SMOOTH ON SKIN BEFORE OR AFTER MAKEUP
Warnings
KEEP OUT OF EYES. STOP USE IF IRRITATION OCCURS. KEEP OUT OF REACH OF CHILDREN.
Package Label.Principal Display Panel
BOBBI BROWN
BRIGHTENING
SPF 50 UV
PROTECTIVE FACE BASE
1.7 OZ/50 ML
DIST. BOBBI BROWN PROFESSIONAL COSMETICS
NEW YORK, NY 10022
Folding Carton (E5ypcarton)
* Please review the disclaimer below.
