Home NDC 64141-032-01 BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 30
Product NDC 64141-032
Requested package NDC 64141-032-01
11-digit product format 641410032
Labeler code 64141
Product ID 64141-032_296b2a1e-0a09-3759-e063-6294a90a7912
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, TITANIUM DIOXIDE and ZINC OXIDE
Dosage form LIQUID
Route TOPICAL
Labeler Bobbi Brown Professional Cosmetics Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-04-12
Substance OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 67; 21; 13 mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 67 mg/mL TITANIUM DIOXIDE 21 mg/mL ZINC OXIDE 13 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 15FIX9V2JP Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64141-032-01 BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 30 30 mL in 1 BOTTLE LIQUID 30 8 64141-032-01 BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 30 1 in 1 CARTON LIQUID 1 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64141-032 BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 30 (OCTINOXATE, TITANIUM DIOXIDE AND ZINC OXIDE) LIQUID [BOBBI BROWN PROFESSIONAL COSMETICS INC.] 8 Current NDC, Legacy NDC, 2 package rows 20241218_1f9a4b71-45aa-4156-9fe6-ffa81f808a85.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 242 of 353 · 7,041 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 64141-032-01 64141003201 1 BOTTLE in 1 CARTON (64141-032-01) / 30 mL in 1 BOTTLE 1 bottle 2021-04-12 0000-00-00 No No Current