Obagi Skintrinsiq Clarifiying Protocol

Product NDC: 62032-909
11-digit product format: 620320909
Labeler code: 62032
Product ID: 62032-909_a9c17c57-a3af-43d6-9db3-56fb8e28894b
Type: HUMAN OTC DRUG
Nonproprietary name: salicylic acid, titanium dioxide, and zinc oxide
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: 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 · 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	62032-909-09	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	62032-909-09	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	62032-909-09	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	62032-909-09	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	62032-909-09	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	62032-909-09	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	62032-909-09	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 Clarifiying Protocol
Listing expiration: 2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
251577	Internal RxNorm lookup
1235208	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
08ba9ea8-73fd-472b-9cc4-67df167352ec	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62032-612-04	Obagi Skintrinsiq Clarifiying Protocol	148 mL in 1 BOTTLE, PLASTIC	LIQUID	148 mL	20 mg in 1mL	3
62032-811-09	Obagi Skintrinsiq Clarifiying Protocol	1 in 1 CARTON	LOTION		15.6 g in 100g	3
62032-811-09	Obagi Skintrinsiq Clarifiying Protocol	85 g in 1 TUBE	LOTION	85 g	15.6 g in 100g	3
62032-909-09	Obagi Skintrinsiq Clarifiying Protocol	1 in 1 BOX	KIT	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62032-909	OBAGI SKINTRINSIQ CLARIFIYING PROTOCOL (SALICYLIC ACID, TITANIUM DIOXIDE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC]	3	Current NDC, Legacy NDC, 4 package rows	20250406_08ba9ea8-73fd-472b-9cc4-67df167352ec.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 58 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2000DL-CL30T	SPF30 BS TROPICAL	Epic Laboratories, LLC	0286f94e-a2e8-b529-e063-6294a90ac08d	2026-03-02	Warnings	Exact identifier application number: M020
2000DL-CL30V	SPF30 BS ORIGINAL	Epic Laboratories, LLC	1872eefd-d702-ac9f-e063-6294a90a24ef	2026-03-02	Warnings	Exact identifier application number: M020
JAYSUING White Birch Moisturizing Sunscreen Cream	TITANIUM DIOXIDE	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	4c174691-cc32-b2e4-e063-6294a90a0f73	2026-03-02	Warnings	Exact identifier application number: M020
Kypris Pot of Shade Heliotropic Broad Spectrum SPF 30 Sunscreen And Primer	ZINC OXIDE	Kypris Beauty LLC	a5d5f7bd-d7bf-4a5c-8530-b9d5d74754c3	2026-02-27	Warnings	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Chain Drug Marketing Association	6307627a-94e2-47ea-8519-68975716dd6e	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Sport Sunscreen SPF 30	AVEBONZONE, HOMOSALATE, OCTISALATE	Chain Drug Marketing Association	a38e150e-2e50-4936-ae46-408f9cf82d15	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Sport Sunscreen SPF 70	AVOBENZONE, HOMOSALATE, OCTISALATE	Chain Drug Marketing Association	87811c86-19d2-4179-8d22-2aeb4680ff57	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Sunscreen for Kids SPF 50	AVEBONZONE, HOMOSALATE, OCTISALATE	Chain Drug Marketing Association	d7215a32-00a9-4b70-8597-8ea91f546c1e	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Sport Sunscreen SPF 50	AVEBONZONE, HOMOSALATE, OCTISALATE	Chain Drug Marketing Association	9fccccd4-2d2e-4812-85b1-bbeb44ff04ea	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	The Kroger Co.	be702a3b-1652-4468-803d-295100d3e3e2	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	The Kroger Co.	644ec129-15c9-4ac1-8362-5b4c2e58ab9a	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
SPF Beauty	SPF BEAUTY	Walmart Inc.	f06f26af-81d6-4603-b377-fd12430ec952	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
SPF Moisturizer	SPF MOISTURIZER	Walmart Inc.	41de3171-9ed3-45da-96fb-dfcf41912229	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Facial Moisturizer	DAILY FACIAL MOISTURIZER SPF 15	Walmart Inc.	2cec9c90-2e64-f005-e063-6294a90a8753	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Walmart Inc.	309d881d-40e0-37bc-e063-6294a90a3769	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M020
Avbenzone, Homosalate, Octisalate	AVBENZONE, HOMOSALATE, OCTISALATE	Walmart Inc.	d3d7a5d3-5c78-45c3-ba4b-7ac1a3b4526a	2026-02-27	Warnings	Exact identifier application number: M020
MELAO Sunscreen Stick	ETHYLHEXYL METHOXYCINNAMATE, HOMOSALATE, OCTOCRYLENE, AVOBENZONE	Guangdong Aimu Biological Technology Co., Ltd	4ba15c03-0409-918b-e063-6294a90ac6ee	2026-02-26	Warnings	Exact identifier application number: M020
TIBENA EVERY DAY REAL SUN BLOCK	TITANIUM DIOXIDE, ZINC OXIDE	KONAD CO LTD	211c9930-4f91-cf8f-e063-6394a90a97b3	2026-02-26	Warnings	Exact identifier application number: M020
Olay Regenerist Whip Lightweight Moisturizer with Sunscreen Broad Spectrum SPF 25	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	4bbc0639-3a80-1c28-e063-6394a90a3c00	2026-02-26	Warnings	Exact identifier application number: M020
CLE DE PEAU BEAUTE RADIANT FLUID FOUNDATION MATTE M B10	TITANIUM DIOXIDE	Shiseido Americas Corporation	54f8210f-4934-4ada-89c3-aa89e7a09260	2026-02-26	Warnings	Exact identifier application number: M020

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1235208	CLENZIderm M.D. 2 % Pore Therapy Topical Solution	PSN	08ba9ea8-73fd-472b-9cc4-67df167352ec	3
251577	salicylic acid 2 % Topical Solution	PSN	08ba9ea8-73fd-472b-9cc4-67df167352ec	3
1235208	salicylic acid 20 MG/ML Topical Solution [Clenziderm]	SBD	08ba9ea8-73fd-472b-9cc4-67df167352ec	3
251577	salicylic acid 20 MG/ML Topical Solution	SCD	08ba9ea8-73fd-472b-9cc4-67df167352ec	3
1235208	Clenziderm 20 MG/ML Topical Solution	SY	08ba9ea8-73fd-472b-9cc4-67df167352ec	3
1235208	Clenziderm M.D. 2 % Pore Therapy	SY	08ba9ea8-73fd-472b-9cc4-67df167352ec	3
251577	salicylic acid 2 % Topical Solution	SY	08ba9ea8-73fd-472b-9cc4-67df167352ec	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
62032-612-04	62032061204	148 mL in 1 BOTTLE, PLASTIC	148 ml					Historical
62032-811-09	62032081109	1 in 1 CARTON						Historical
62032-909-09	62032090909	1 KIT in 1 BOX (62032-909-09) * 148 mL in 1 BOTTLE, PLASTIC (62032-612-04) * 1 BOTTLE, PUMP in 1 CARTON / 48 g in 1 BOTTLE, PUMP * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 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™ Clarifiying Protocol Kit	Obagi Cosmeceuticals LLC \| G.S.COSMECEUTICAL USA, INC. \| Denison Pharmaceuticals, LLC \| Swiss-American CDMO, LLC \| TENCO ASSEMBLIES, INC	2025-03-21	HUMAN OTC DRUG LABEL	3