Obagi Skintrinsiq Antioxidant Protocol

Product NDC: 62032-907
11-digit product format: 620320907
Labeler code: 62032
Product ID: 62032-907_8299732b-f96d-45fe-ae06-058f296cad1e
Type: HUMAN OTC DRUG
Nonproprietary name: AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE
Dosage form: KIT
Labeler: Obagi Cosmeceuticals LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-08-01
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	62032-907	62032-907-07	D	Discontinued by firm		2026-11-13

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 · 14 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	62032-907-07	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	62032-907-07	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	62032-907-07	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	62032-907-07	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	62032-907-07	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	62032-907-07	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62032-907-07	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Obagi Skintrinsiq Antioxidant Protocol
Listing expiration: 2027-12-31

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
495bc176-b292-448f-a5a6-00de2e475e54	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7	Product name	1	20171122

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-04-01	Obagi ® Skintrinsiq™ Antioxidant Protocol Kit 15%
2025-01-30	Obagi ® Skintrinsiq™ Antioxidant Protocol Kit 15%
2023-03-29	Obagi ® Skintrinsiq™ Antioxidant Protocol Kit 15%
2023-01-30	Obagi ® Skintrinsiq™ Antioxidant Protocol Kit 15%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62032-050-54	Obagi Skintrinsiq Antioxidant Protocol	1 in 1 CARTON	CREAM		80 mg in 1g	4
62032-050-54	Obagi Skintrinsiq Antioxidant Protocol	48 g in 1 TUBE	CREAM	48 g	80 mg in 1g	4
62032-907-07	Obagi Skintrinsiq Antioxidant Protocol	1 in 1 BOX	KIT	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62032-907	OBAGI SKINTRINSIQ ANTIOXIDANT PROTOCOL (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) KIT [OBAGI COSMECEUTICALS LLC]	3	Current NDC, Legacy NDC, 3 package rows	20250406_495bc176-b292-448f-a5a6-00de2e475e54.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 322 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
YOU-V SPF-30 Broad Spectrum Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	YouV, LLC	290cd617-aa90-4f10-8a1d-d8954b927004	2023-11-11	Warnings	Exact identifier application number: M020
BEAST SPIT and POLISH FACE SPF-20	OCTOCRYLENE, OCTISALATE, AVOBENZONE	Small Batch Beauty, LLC	27e5244b-4b69-4dec-9dd5-ba8b71b171b2	2023-11-11	Warnings	Exact identifier application number: M020
SEVEN MINERALS Skin Friendly SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Seven Minerals NA LLC	bd60cf89-e0e9-48ad-b174-1ecf72557d9c	2023-11-11	Warnings	Exact identifier application number: M020
OUTER REEF Reef Safe (WR) Broad Spectrum SPF 30	TITANIUM DIOXIDE	Coral Reef Park Co., Inc.	743f3d23-0f5c-4724-9f69-411c109506e1	2023-11-11	Warnings	Exact identifier application number: M020
SEVEN MINERALS Skin Friendly SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Seven Minerals NA LLC	6d6b5b2a-210a-4606-9cdb-f6eec10f37e8	2023-11-11	Warnings	Exact identifier application number: M020
KISS MY FACE SPF-50 Baby Mineral Sunscreen	ZINC OXIDE	WINDMILL HEALTH PRODUCTS LLC	ac66ad82-a01f-4e44-92a7-b5ab5bd30922	2023-11-11	Warnings	Exact identifier application number: M020
KISS MY FACE SPF-50 Daily Mineral Sunscreen	ZINC OXIDE	WINDMILL HEALTH PRODUCTS LLC	1745dc35-648e-4315-a285-c99ebeef4f6a	2023-11-11	Warnings	Exact identifier application number: M020
KISS MY FACE SPF-50 Face Factor Mineral Sunscreen	ZINC OXIDE	WINDMILL HEALTH PRODUCTS LLC	edc2c1e7-e1a8-4b49-96df-8a94eb6a242a	2023-11-11	Warnings	Exact identifier application number: M020
ONCODERM Rx Mineral Sunscreen SPF-30	TITANIUM DIOXIDE, ZINC OXIDE	Oncoderm, LLC	9f16e832-067c-4ae8-bd7d-6f0dc0ad6fae	2023-11-11	Warnings	Exact identifier application number: M020
SEAWEED BATH CO. SPF 50 SPORT	OCTOCRYLENE, ZINC OXIDE, OCTISALATE	The Seaweed Bath Co.	f01516bf-8aed-4402-a3f9-ef11c54d46b3	2023-11-11	Warnings	Exact identifier application number: M020
SEAWEED BATH CO. SPF-30	OCTOCRYLENE, ZINC OXIDE, OCTISALATE	The Seaweed Bath Co.	4df55434-fb9a-442d-82cf-16a4957f0a2a	2023-11-11	Warnings	Exact identifier application number: M020
PROJECT REEF Mineral Sunscreen SPF-30	ZINC OXIDE	Project Reef LLC	b7de9ec2-6db1-4c89-b734-15c4bd5c3251	2023-11-11	Warnings	Exact identifier application number: M020
SEAWEED BATH CO Cooling Mist SPF-60 Sport	HOMOSALATE, OCTISALATE, ZINC OXIDE	The Seaweed Bath Co.	98ccbb70-6e1a-4e92-a095-cbc4be12fcbf	2023-11-11	Warnings	Exact identifier application number: M020
PROJECT REEF Mineral Sunscreen SPF-50	ZINC OXIDE, TITANIUM DIOXIDE	Project Reef LLC	87b9170c-956e-4aa2-9416-da00cca81b58	2023-11-11	Warnings	Exact identifier application number: M020
YOUTH CORRIDOR Soothe and Defend SPF-30	OCTOCRYLENE, OCTISALATE, ZINC OXIDE	Youth Corridor	5c0873ff-8e76-48de-919d-f69794c4bd37	2023-11-11	Warnings	Exact identifier application number: M020
ZITSTICKA MEGASHADE SUNSCREEN SERUM (SPF-50)	HOMOSALATE, OCTINOXATE, OCTISALATE, ZINC OXIDE	ZITSTICKA, Inc	32164318-7a7e-40b2-99da-8246c99fdbd3	2023-11-11	Warnings	Exact identifier application number: M020
SUNNY Q Broad Spectrum SPF-30	ZINC OXIDE	Sunny Q Sunscreen LLC	593870fa-425c-401c-ac26-f63f4ce0298f	2023-11-11	Warnings	Exact identifier application number: M020
BRICKELL Daily Defense Face Moisturizer SPF-20	OCTISALATE, ZINC OXIDE	BRICKELL BRANDS LLC	44806b83-9220-4d34-806d-20cf0a47186e	2023-11-11	Warnings	Exact identifier application number: M020
BRICKELL Element Defense Moisturizer SPF-45	OCTOCRYLENE, OCTISALATE, ZINC OXIDE	BRICKELL BRANDS LLC	94be278a-3773-469b-8e40-3242d1072a3d	2023-11-11	Warnings	Exact identifier application number: M020
I KNOW Very Necessary Broad Spectrum SPF-40 Moisturizing Cream	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Thirty7 LLC	6ff00b6e-1cc7-4cc4-842b-4e379f75e454	2023-11-11	Warnings	Exact identifier application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
62032-050-54	62032005054	1 in 1 CARTON						Historical
62032-907-07	62032090707	1 KIT in 1 BOX (62032-907-07) * 1 BOTTLE, DROPPER in 1 CARTON > 30 mL in 1 BOTTLE, DROPPER * 1 BOTTLE, PUMP in 1 CARTON > 30 mL in 1 BOTTLE, PUMP * 1 BOTTLE, PUMP in 1 CARTON > 48 g in 1 BOTTLE, PUMP * 59 mL in 1 BOTTLE, PLASTIC * 60 mL in 1 BOTTLE, PLASTIC	1 kit	2021-08-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Obagi ® Skintrinsiq™ Antioxidant Protocol Kit 15%	Obagi Cosmeceuticals LLC \| G.S.COSMECEUTICAL USA, INC. \| Denison Pharmaceuticals, LLC \| Swiss-American CDMO, LLC \| TENCO ASSEMBLIES, INC	2026-04-27	HUMAN OTC DRUG LABEL	4