Home NDC 64141-031 BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40
Product NDC 64141-031
11-digit product format 641410031
Labeler code 64141
Product ID 64141-031_296a93aa-91b1-00b2-e063-6394a90a0086
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 2021-01-27
Substance OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 40; 62; 39 mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-27 05:24 UTC · source 2025-02-26 unfinished product product f268b84574a6…26285f5ac5df…2025-02-01 13:13 UTC · source 2025-01-31 unfinished product product f764e8902f78…92046438deef…2025-01-20 13:05 UTC · source 2025-01-17 unfinished product product 68b1e3bced9e…98a755eb8bc6…2024-11-29 20:42 UTC · source 2024-11-29 unfinished product product 05c55d027831…ca05dca9dc4c…2024-11-29 20:42 UTC · source 2024-11-29 unfinished package package 64141-031-00 05c55d027831…ca05dca9dc4c…2024-11-09 02:36 UTC · source 2024-11-08 unfinished product product 48b4f40e6753…c7c7a00d2afa…2024-11-09 02:36 UTC · source 2024-11-08 unfinished package package 64141-031-00 48b4f40e6753…c7c7a00d2afa…2024-10-09 02:27 UTC · source 2024-10-08 unfinished product product 27f29a85d7e4…1372111e901f…2024-10-09 02:27 UTC · source 2024-10-08 unfinished package package 64141-031-00 27f29a85d7e4…1372111e901f…2024-07-10 04:00 UTC · source 2024-07-09 unfinished product product 8d62ce987f31…9fe9ef23e30d…2024-07-10 04:00 UTC · source 2024-07-09 unfinished package package 64141-031-00 8d62ce987f31…9fe9ef23e30d…2024-05-28 21:11 UTC · source 2024-05-28 unfinished product product d1e113ab4d42…063ee3eb0a1d…2024-05-28 21:11 UTC · source 2024-05-28 unfinished package package 64141-031-00 d1e113ab4d42…063ee3eb0a1d…2024-05-15 03:51 UTC · source 2024-05-14 unfinished product product 50b4072663b7…eae3003ed65e…2024-05-15 03:51 UTC · source 2024-05-14 unfinished package package 64141-031-00 50b4072663b7…eae3003ed65e…
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 40
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 40 mg/mL TITANIUM DIOXIDE 62 mg/mL ZINC OXIDE 39 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 64141-031-01 BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40 30 mL in 1 BOTTLE LIQUID 30 7 64141-031-01 BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40 1 in 1 CARTON LIQUID 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64141-031 BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40 (OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LIQUID [BOBBI BROWN PROFESSIONAL COSMETICS INC.] 7 Current NDC, Legacy NDC, 2 package rows 20241218_dc6b28ca-b922-460a-8028-fb3f5afdbe9d.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 26 of 357 · 7,139 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 64141-031-01 64141003101 1 BOTTLE in 1 CARTON (64141-031-01) / 30 mL in 1 BOTTLE 1 bottle 2021-01-27 0000-00-00 No No Current