SUN SHIELD BROAD SPECTRUM SPF 50 MATTE

Product NDC: 62032-140
11-digit product format: 620320140
Labeler code: 62032
Product ID: 62032-140_7415289e-2b1a-416a-ab5d-2fafa7059e17
Type: HUMAN OTC DRUG
Nonproprietary name: HOMOSALATE, OCTISALATE, and ZINC OXIDE
Dosage form: LOTION
Route: TOPICAL
Labeler: Obagi Cosmeceuticals LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-07-15
Substance: HOMOSALATE; OCTISALATE; ZINC OXIDE
Active strength: 100; 50; 165 mg/g; mg/g; mg/g
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 · 32 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
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	62032-140-34	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	62032-140-05	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	62032-140-09	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
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	62032-140-34	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	62032-140-05	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	62032-140-09	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	62032-140-34	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	62032-140-05	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	62032-140-09	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	62032-140-34	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	62032-140-05	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	62032-140-09	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	62032-140-34	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	62032-140-05	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	62032-140-09	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	62032-140-34	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	62032-140-09	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	62032-140-05	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	62032-140-34	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	62032-140-09	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	62032-140-05	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	62032-140-34	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62032-140-09	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62032-140-05	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: SUN SHIELD BROAD SPECTRUM SPF 50 MATTE
Brand name suffix: SUNSCREEN
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
HOMOSALATE	100 mg/g
OCTISALATE	50 mg/g
ZINC OXIDE	165 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
V06SV4M95S	Internal UNII lookup
4X49Y0596W	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
263ef8e8-e0c4-42e6-bb26-7581a437b35a	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
c5cd4727-ac49-4409-82b1-5bd8006c3ec7	Product name	1	20171122
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
1681bc73-b05f-12c3-1075-382ae39f449c	Product name	1	20140508
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
85490a6b-2306-6bf2-c51b-eb63537dc2da	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
b060cc1a-fe47-856b-0b77-4448b5963de8	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
62032-140-05	2025-10-02	SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-09	2025-10-02	SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-34	2025-10-02	SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-05	2025-01-30	SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-09	2025-01-30	SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-34	2025-01-30	SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62032-140-05	SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN	28 g in 1 TUBE	LOTION	28		5
62032-140-09	SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN	1 in 1 CARTON	LOTION	1		5
62032-140-09	SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN	85 g in 1 TUBE	LOTION	85		5
62032-140-34	SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN	479 g in 1 BOTTLE, PUMP	LOTION	479		5
62032-140-09	Obagi Nu-Derm System Normal-Dry Skin Transformation Kit	85 g in 1 TUBE	LOTION	85 g	165 mg in 1g	4
62032-140-09	Obagi Nu-Derm Fx System Normal-Oily Skin TransformationComplexion Brightening System	85 g in 1 TUBE	LOTION	85 g	165 mg in 1g	4
62032-140-09	Obagi Nu-Derm Fx System Normal-Oily Skin TransformationComplexion Brightening System	1 in 1 CARTON	LOTION		50 mg in 1g	4
62032-140-09	Obagi Nu-Derm System Normal-Oily Skin Transformation	85 g in 1 TUBE	LOTION	85 g	50 mg in 1g	4
62032-140-09	Obagi Nu-Derm System Normal-Dry Skin Transformation Kit	1 in 1 CARTON	LOTION		50 mg in 1g	4
62032-140-09	Obagi Nu-Derm System Normal-Oily Skin Transformation	1 in 1 CARTON	LOTION		100 mg in 1g	4
62032-140-05	Obagi Nu-Derm System Normal-Oily Skin Transformation Trial	28 g in 1 TUBE	LOTION	28 g	100 mg in 1g	3
62032-140-05	Obagi Nu-Derm System Normal-Dry Skin Transformation Trial	28 g in 1 TUBE	LOTION	28 g	50 mg in 1g	3
62032-140-09	Obagi Skintrinsiq Brightening Protocol	1 in 1 CARTON	LOTION		100 mg in 1g	3
62032-140-09	Obagi Skintrinsiq Brightening Protocol	85 g in 1 TUBE	LOTION	85 g	50 mg in 1g	3
62032-140-09	Obagi-C C-Rx System Normal-Dry Skin Intervention	1 in 1 CARTON	LOTION		100 mg in 1g	3
62032-140-09	Obagi-C C-Rx System Normal-Dry Skin Intervention	85 g in 1 TUBE	LOTION	85 g	50 mg in 1g	3
62032-140-09	Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin	85 g in 1 TUBE	LOTION	85 g	100 mg in 1g	3
62032-140-09	Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System	1 in 1 CARTON	LOTION		50 mg in 1g	3
62032-140-09	Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin	1 in 1 CARTON	LOTION		100 mg in 1g	3
62032-140-09	Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System	85 g in 1 TUBE	LOTION	85 g	50 mg in 1g	3
62032-140-05	Obagi Medical Way to Glow Kit	28 g in 1 TUBE	LOTION	28 g	50 mg in 1g	2
62032-140-09	Obagi-C C-Rx System Normal-Oily Skin Intervention	85 g in 1 TUBE	LOTION	85 g	50 mg in 1g	1
62032-140-09	Obagi-C C-Rx System Normal-Oily Skin Intervention	1 in 1 CARTON	LOTION		50 mg in 1g	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62032-140	OBAGI SKINTRINSIQ BRIGHTENING PROTOCOL (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC]	3	Current NDC, Legacy NDC	20250406_2f75ebf7-d6b6-45c6-ad5b-61739d260ff7.zip
62032-140	OBAGI MEDICAL WAY TO GLOW KIT (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC]	2	Current NDC, Legacy NDC	20250406_f6f6e219-4ef6-be3b-e053-6294a90a660d.zip
62032-140	SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) LOTION [OBAGI COSMECEUTICALS LLC]	2	Current NDC, Legacy NDC, 4 package rows	20191102_263ef8e8-e0c4-42e6-bb26-7581a437b35a.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 94 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eucerin Sensitive Mineral Face Sunscreen SPF 35	ZINC OXIDE 24%	Beiersdorf Inc	f3a8bb6b-f051-5d39-e053-2a95a90adafc	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Limited Edition Sunscreen SPF 30	AVOBENZONE 2%, HOMOSALATE 8%, OCTISALATE 4.5%, OCTOCRYLENE 7%	Beiersdorf Inc	f41e09bf-407d-65a4-e053-2a95a90a2436	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Glow Hydragel SPF 50	AVOBENZONE 3%, HOMOSALATE 9%, OCTISALATE 4.5%, OCTOCRYLENE 9%	Beiersdort Inc	b5f7cacb-92b9-a6b7-e053-2a95a90aea02	2025-12-31	Warnings	Exact identifier application number: M020
Eucerin Advanced Hydration Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Beiersdorf Inc	cd6112fe-89e4-a79b-e053-2a95a90ad7f4	2025-12-31	Warnings	Exact identifier application number: M020
Eucerin Age Defense SPF 50 Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Beiersdort Inc	cd9d4f30-fb37-9935-e053-2995a90a9936	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Sport Sunscreen SPF 70	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%, OXYBENZONE 6%	Beiersdorf Inc	cc5d1f9b-2c8a-1392-e053-2a95a90acb9e	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Every Tone Brightening Sunscreen SPF 60	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Beiersdorf Inc	23e368db-4b2f-d23b-e063-6394a90a1f06	2025-12-31	Warnings	Exact identifier application number: M020
Eucerin Advanced Hydration Ultra-Light Face Sunscreen SPF 50	AVOBENZENE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 10%	Beiersdorf Inc	25d9c520-431a-5546-e063-6394a90a4e0d	2025-12-31	Warnings	Exact identifier application number: M020
Eucerin Advanced Hydration Sunscreen SPF 30	(TO DELIVER) AVOBENZONE 3%, HOMOSALATE 7%, OCTISALATE 4.5%, OCTOCRYLENE 8%	Beiersdorf Inc	1273012a-107c-1b19-e063-6394a90a53e4	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Every Tone Face Hydrating Clear Sunscreen SPF 60	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Beiersdorf Inc	23e5bf2c-88c2-d346-e063-6394a90abc78	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Every Tone Invisible Clear Sunscreen Stick SPF 55	AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 10%	Beiersdorf Inc	23fb728a-8c11-d041-e063-6294a90abb55	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Kids Sport Sunscreen SPF 50	AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 5%	Beiersdorf Inc	c0421c97-72bd-fcac-e053-2995a90aac28	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Defend and Clear	OCTINOXATE, OCTISALATE, ZINC OXIDE	Beiersdorf Inc	baaec6a9-2c60-2d11-e053-2a95a90abca7	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Pure and Simple Sunscreen SPF 50	ZINC OXIDE 24.08%	Beiersdorf Inc	b6492438-5dd2-030e-e053-2a95a90a2f9f	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Sport Sunscreen SPF 30	AVOBENZONE 2%, HOMOSALATE 8%, OCTISALATE 4.5%, OCTOCRYLENE 7%	Beiersdort Inc	ca8d2e20-c1f1-ecf2-e053-2a95a90a790f	2025-12-31	Warnings	Exact identifier application number: M020
Eucerin Tinted Age Defense Suncreen SPF 50	AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 10%	Beiersdorf Inc	125d053c-9418-5772-e063-6294a90a6d6d	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Sport SPF 15 Sunscreen	AVOBENZONE 2%, OCTISALATE 4.5%, OCTOCRYLENE 7%	Beiersdorf Inc	cc4812da-0686-7789-e053-2995a90a561f	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Sport Mineral Sunscreen SPF 50	ZINC OXIDE	Beiersdorf Inc	b6861830-fdad-3829-e053-2a95a90a0971	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Kids Tear Free Mineral Sunscreen SPF 50	OCTINOXATE 7.5%, OCTISALATE 5%, ZINC OXIDE 14.5%	Beiersdorf Inc	c054fd86-b0d9-24fc-e053-2a95a90aea2c	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Kids Sunscreen SPF 70	AVOBENZONE 3%, HOMOSALATE 13%, OCTISALATE 5%, OCTOCRYLENE 10%, OXYBENZONE 6%	Beiersdorf Inc	c0552256-d8cb-5473-e053-2995a90ad0d5	2025-12-31	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
197795	hydroquinone 4 % Topical Cream	PSN	16efa2db-8172-4026-a519-08f53d68b3c9	4
197795	hydroquinone 4 % Topical Cream	PSN	e63327db-fb96-411c-945a-abe801d38045	4
197795	hydroquinone 40 MG/ML Topical Cream	SCD	16efa2db-8172-4026-a519-08f53d68b3c9	4
197795	hydroquinone 40 MG/ML Topical Cream	SCD	e63327db-fb96-411c-945a-abe801d38045	4
197795	hydroquinone 4 % Topical Cream	SY	16efa2db-8172-4026-a519-08f53d68b3c9	4
197795	hydroquinone 4 % Topical Cream	SY	e63327db-fb96-411c-945a-abe801d38045	4
197795	hydroquinone 4 % Topical Cream	PSN	ca931d1c-4df4-47ce-8d5c-cd8c3e38c02b	3
197795	hydroquinone 4 % Topical Cream	PSN	e2c23345-69df-47a1-8e6b-b6225080d363	3
197795	hydroquinone 4 % Topical Cream	PSN	219c68dc-1e74-4136-9065-85466008d445	3
197795	hydroquinone 40 MG/ML Topical Cream	SCD	ca931d1c-4df4-47ce-8d5c-cd8c3e38c02b	3
197795	hydroquinone 40 MG/ML Topical Cream	SCD	e2c23345-69df-47a1-8e6b-b6225080d363	3
197795	hydroquinone 40 MG/ML Topical Cream	SCD	219c68dc-1e74-4136-9065-85466008d445	3
197795	hydroquinone 4 % Topical Cream	SY	ca931d1c-4df4-47ce-8d5c-cd8c3e38c02b	3
197795	hydroquinone 4 % Topical Cream	SY	e2c23345-69df-47a1-8e6b-b6225080d363	3
197795	hydroquinone 4 % Topical Cream	SY	219c68dc-1e74-4136-9065-85466008d445	3
197795	hydroquinone 4 % Topical Cream	PSN	e19b824f-4438-48c8-af4c-29be197f9cdc	1
197795	hydroquinone 40 MG/ML Topical Cream	SCD	e19b824f-4438-48c8-af4c-29be197f9cdc	1
197795	hydroquinone 4 % Topical Cream	SY	e19b824f-4438-48c8-af4c-29be197f9cdc	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
62032-140-05	62032014005	28 g in 1 TUBE (62032-140-05)	28 g	2019-07-15	0000-00-00	No	No	Current
62032-140-09	62032014009	1 TUBE in 1 CARTON (62032-140-09) / 85 g in 1 TUBE	1 tube	2019-07-15	0000-00-00	No	No	Current
62032-140-34	62032014034	479 g in 1 BOTTLE, PUMP (62032-140-34)	479 g	2019-07-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Obagi-C ® Fx System Normal-Oily Skin Brightening System with Arbutin	Obagi Cosmeceuticals LLC \| Bay Cities Container Corporation \| Swiss American CDMO, LLC \| Universal Packaging Systems, Inc. (DBA Paklab)	2026-01-26	HUMAN OTC DRUG LABEL	3
Obagi-C ® C-Rx System Normal-Dry Skin Intervention	Obagi Cosmeceuticals LLC \| Bay Cities Container Corporation \| G. S. Cosmeceutical USA, Inc. \| Swiss American CDMO, LLC \| PURETEK CORPORATION	2026-01-26	HUMAN OTC DRUG LABEL	3
Obagi Nu-Derm ® System Normal-Dry Skin Transformation Kit	Obagi Cosmeceuticals LLC \| Swiss-American CDMO, LLC \| G.S.COSMECEUTICAL USA, INC. \| Bay Cities Container Corporation	2025-10-23	HUMAN PRESCRIPTION DRUG LABEL	4
Homosalate, Octisalate, Zinc Oxide	Obagi Cosmeceuticals LLC \| Bay Cities Container Corporation \| Swiss American CDMO, LLC \| G. S. Cosmeceutical USA, Inc.	2025-10-23	HUMAN OTC DRUG LABEL	4
Obagi ® Nu-Derm ® System Normal-Oily Skin Transformation	Obagi Cosmeceuticals LLC \| Bay Cities Container Corporation \| G. S. Cosmeceutical USA, Inc. \| Swiss American CDMO, LLC	2025-10-23	HUMAN PRESCRIPTION DRUG LABEL	4
Obagi Nu-Derm ® System Normal-Oily Skin Transformation Trial	Obagi Cosmeceuticals LLC \| G. S. Cosmeceutical USA, Inc. \| Swiss American CDMO, LLC \| Bay Cities Container Corporation	2025-10-23	HUMAN PRESCRIPTION DRUG LABEL	3
Homosalate, Octisalate, Zinc Oxide	Obagi Cosmeceuticals LLC \| Bay Cities Container Corporation \| Swiss American CDMO, LLC \| G. S. Cosmeceutical USA, Inc.	2025-10-23	HUMAN OTC DRUG LABEL	3
Obagi ® Nu-Derm ® System Normal-Dry Skin Transformation Trial	Obagi Cosmeceuticals LLC \| Swiss American CDMO, LLC \| G. S. Cosmeceutical USA, Inc. \| Bay Cities Container Corporation	2025-10-23	HUMAN OTC DRUG LABEL	3
Obagi-C ® C-Rx System Normal-Oily Skin Intervention	Obagi Cosmeceuticals LLC \| Bay Cities Container Corporation \| G. S. Cosmeceutical USA, Inc. \| Swiss American CDMO, LLC \| Universal Packaging Systems, Inc. (DBA Paklab) \| PURETEK CORPORATION	2025-10-21	HUMAN OTC DRUG LABEL	1
Obagi ® Skintrinsiq Brightening 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
Obagi Medical Way to Glow Kit	Obagi Cosmeceuticals LLC \| G.S.COSMECEUTICAL USA, INC. \| Denison Pharmaceuticals, LLC \| Swiss-American CDMO, LLC \| Identipak, Inc.	2025-03-20	HUMAN OTC DRUG LABEL	2
SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION	Obagi Cosmeceuticals LLC \| Swiss-American CDMO, LLC	2025-03-14	HUMAN OTC DRUG LABEL	5