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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
dc6b28ca-b922-460a-8028-fb3f5afdbe9d	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64141-031-01	2022-08-04	C162847	48780-1	e4f33bdf-9d7d-d8a0-e053-dadaa90a6e4e	BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40
64141-031-01	2022-07-29	C162847	48780-1	e4f33bdf-9d7d-d8a0-e053-dadaa90a6e4e	BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40

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 237 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Baby Donna SHeer SPF Sunscreen Stick	ZINC OXIDE	Stream2Sea, LLC	a1b1cdeb-e5fe-4ba1-8bb0-3c7a97dd93fe	2025-01-12	Warnings	Exact identifier application number: M020
SUN PROTECT LIP BALM SPF 30	ZINC OXIDE AND TITANIUM DIOXIDE	Stream2Sea, LLC	21386652-b952-48be-b077-1acecc7f0eb0	2025-01-12	Warnings	Exact identifier application number: M020
Equate Beauty Daily Moisturizer SPF-30 Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE	Wal-Mart Stores, Inc.	00abd6d0-c467-4885-80fe-b062622147d7	2025-01-10	Warnings	Exact identifier application number: M020
Bondi Sands SPF 60 Sunny Body	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	BONDI SANDS (USA) INC.	2b5aebed-49f6-7bb8-e063-6294a90a8521	2025-01-10	Warnings	Exact identifier application number: M020
Bondi Sands SPF 60 Sunny Drops Face Serum	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	BONDI SANDS (USA) INC.	2b5c69e4-2819-94ef-e063-6394a90a68e7	2025-01-10	Warnings	Exact identifier application number: M020
Dermaroller Anhydrous Sunscreen SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Owen Biosciences, Inc.	04e82f1b-c893-4795-b7a9-0523e3ec7552	2025-01-10	Warnings	Exact identifier application number: M020
Skinfuse Shield SPF 30	ZINC OXIDE	Owen Biosciences, Inc.	b8e4c11a-4b4f-4e36-a75e-0a73913113d5	2025-01-10	Warnings	Exact identifier application number: M020
Correct and Protect Serum Broad Spectrum SPF 45	ZINC OXIDE	Murad, LLC	60c62108-6806-4722-a44b-f1c300d59c1e	2025-01-10	Warnings	Exact identifier application number: M020
Multi Vitamin Clear Coat Broad Spectrum SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Murad, LLC	e023c874-c89d-4bd0-a0b9-a8161c261457	2025-01-10	Warnings	Exact identifier application number: M020
CoTZ Baby	ZINC OXIDE	Fallien Cosmeceuticals, LTD	17cc12c7-5af8-413f-b205-31ac150583e2	2025-01-09	Warnings	Exact identifier application number: M020
ISNTREE HYALURONIC ACID DAILY SUNGEL	AVOBENZONE, HOMOSALATE, OCTISALATE	ISNTREE Inc.	2b3bdbe1-ede9-cd60-e063-6394a90ab2f3	2025-01-09	Warnings	Exact identifier application number: M020
JAFRA ROYAL REVITALIZE 4 TUBE SET	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Distribuidora Comercial Jafra, S.A. de C.V.	b4a0d6ab-50a7-43e7-9d7e-a4c01d7eca98	2025-01-09	Warnings	Exact identifier application number: M020
glo SKIN BEAUTY Moisturizing Tint SPF 30	GLO SKIN BEAUTY MOISTURIZING TINT SPF 30	Hayden Caleel LLC	2b464a70-8f40-3148-e063-6394a90ac18c	2025-01-09	Warnings	Exact identifier application number: M020
Sunscreen and insect repellent Bull frog	SPF 50	Bullfrog Brands, LLC	d65d15a6-0a32-1203-e053-2995a90aa6c5	2025-01-09	Warnings	Exact identifier application number: M020
Sunscreen and insect repellent Bull frog	SPF 50	Bullfrog Brands, LLC	d5fb3632-24da-2c7a-e053-2a95a90a5081	2025-01-09	Warnings	Exact identifier application number: M020
Protect Tinted Mineral Sunscreen Broad Spectrum SPF 30	TITANIUM DIOXIDE AND ZINC OXIDE	NEW SEASON DERMATOLOGY, PLLC	fecd72a3-c7e5-3dfa-e053-6394a90a7357	2025-01-09	Warnings	Exact identifier application number: M020
ERBORIAN DOUBLE SAMPLE CC CREME CLAIR and DORE SPF 25	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	LABORATOIRES M&L	41b3cf18-dc11-4e1d-802e-5ba25bd87adb	2025-01-09	Warnings	Exact identifier application number: M020
ECLIPSE SPF 50 PERFECTINT BEIGE	TITANIUM DIOXIDE, ZINC OXIDE	SCIENCE OF SKINCARE LLC	b69dda25-372f-15d9-e053-2995a90a8d3e	2025-01-09	Warnings	Exact identifier application number: M020
PerfecTint Powder SPF 40 All Shades	ZINC OXIDE	Science of Skincare	bb26c010-299e-3dc5-e053-2995a90a2c89	2025-01-09	Warnings	Exact identifier application number: M020
Extreme Protect SPF 40 All Shades	ZINC OXIDE, TITANIUM DIOXIDE	Science of Skincare, LLC.	b69db78b-5f0e-8ca2-e053-2a95a90ac88c	2025-01-09	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40	Bobbi Brown Professional Cosmetics Inc. \| Estee Lauder Companies Inc. \| Estee Lauder Cosmetics Ltd.	2024-12-16	HUMAN OTC DRUG LABEL	7