Obagi Medical Way to Glow Kit

Product NDC: 62032-690
11-digit product format: 620320690
Labeler code: 62032
Product ID: 62032-690_a31ef1ba-8304-4d3f-a030-7fac7224faec
Type: HUMAN OTC DRUG
Nonproprietary name: homosalate, octisalate, and zinc oxide
Dosage form: KIT
Labeler: Obagi Cosmeceuticals LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-03-20
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	62032-690-02	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	62032-690-02	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	62032-690-02	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	62032-690-02	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	62032-690-02	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	62032-690-02	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	62032-690-02	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 Medical Way to Glow Kit
Listing expiration: 2026-12-31

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
f6f6e219-4ef6-be3b-e053-6294a90a660d	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62032-690-02	2025-04-01	C162847	48780-1	2cef2736-818e-d83d-e063-dadaa90ab31f	Obagi Medical Way to Glow Kit
62032-690-02	2025-01-30	C162847	48780-1	2cef2736-818e-d83d-e063-dadaa90ab31f	Obagi Medical Way to Glow Kit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62032-140-05	Obagi Medical Way to Glow Kit	28 g in 1 TUBE	LOTION	28 g	50 mg in 1g	2
62032-690-02	Obagi Medical Way to Glow Kit	1 in 1 BAG	KIT	1		2
62032-690-02	Obagi Medical Way to Glow Kit	1 in 1 CARTON	KIT	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62032-690	OBAGI MEDICAL WAY TO GLOW KIT (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC]	2	Current NDC, 3 package rows	20250406_f6f6e219-4ef6-be3b-e053-6294a90a660d.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 133 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
Tinted Mineral Matte CE Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	The Maui Medical Group, Inc	34b72d14-b69b-e9dd-e063-6394a90a748e	2025-12-11	Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	SCIENCE CEUTICALS, LLC	369b20e2-2cad-e047-e063-6294a90a1bba	2025-12-11	Exact identifier application number: M020
Tinted Mineral Matte CE Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	The Maui Medical Group, Inc	34b60880-5fe1-b78f-e063-6294a90a748d	2025-12-11	Exact identifier application number: M020
Sheer Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	The Maui Medical Group, Inc	34b51190-6a6d-c5e0-e063-6394a90ae875	2025-12-11	Exact identifier application number: M020
Tinted Ultra Zinc Face and Body	ZINC OXIDE	LIV BODY AND BEAUTY LLC	374fae34-41b9-4cab-e063-6394a90a9b1d	2025-12-11	Exact identifier application number: M020
Z Bloc	ZINC OXIDE	The Maui Medical Group, Inc	34b64eb5-a91f-de43-e063-6294a90a8043	2025-12-11	Exact identifier application number: M020
Sheer Tinted Sunscreen Stick	TITANIUM DIOXIDE, ZINC OXIDE	The Maui Medical Group, Inc	34b6e8d0-6235-dac2-e063-6394a90afefd	2025-12-11	Exact identifier application number: M020
Tinted Sunscreen Face Primer	TITANIUM DIOXIDE, ZINC OXIDE	LIV BODY AND BEAUTY	374f6b79-2ac4-61cf-e063-6394a90a699b	2025-12-11	Exact identifier application number: M020
Non Tinted Ultra Zinc Face and Body	ZINC OXIDE	LIV BODY AND BEAUTY LLC	375008f2-8dd4-aa31-e063-6394a90a5be8	2025-12-11	Exact identifier application number: M020
Replenishing Daily Protection	ZINC OXIDE	The Maui Medical Group, Inc	34b96d82-7fcf-e452-e063-6394a90a781b	2025-12-11	Exact identifier application number: M020
Daily Sun Defense	TITANIUM DIOXIDE, ZINC OXIDE	LIV BODY AND BEAUTY LLC	3750c2fd-c5cc-fd00-e063-6394a90aeb89	2025-12-11	Exact identifier application number: M020
Non Tinted Ultra Zinc Face and Body	ZINC OXIDE	LIV BODY AND BEAUTY LLC	3750ffbf-a82d-b4b9-e063-6294a90a7d68	2025-12-11	Exact identifier application number: M020
The Block	ZINC OXIDE	ELITE ESTHETICS BY NICOLE CAROLINE LLC	34a6b17e-6e9e-3f2c-e063-6294a90a1c32	2025-12-11	Exact identifier application number: M020
SPF 40 Broad Spectrum Non-Tinted	ZINC OXIDE	Teton Dermatology Holdings, Inc.	35093797-008b-b265-e063-6294a90a9949	2025-12-11	Exact identifier application number: M020
Tinted Zinc Protection	ZINC OXIDE	Teton Dermatology Holdings, Inc.	3508d5a8-9d3c-51d1-e063-6394a90abc8e	2025-12-11	Exact identifier application number: M020
SPF 40 Broad Spectrum	TITANIUM DIOXIDE, ZINC OXIDE	Teton Dermatology Holdings, Inc.	35081ce0-2203-ab86-e063-6294a90aefd5	2025-12-11	Exact identifier application number: M020
Antioxidant SPF	ZINC OXIDE	Teton Dermatology Holdings, Inc.	3509a916-f3e1-9c53-e063-6394a90a5bff	2025-12-11	Exact identifier application number: M020
Ultimate Physical Sunscreen Tinted	ZINC OXIDE	HALEM DERMATOLOGY PLLC	35bb4953-ca8c-e927-e063-6394a90a1a31	2025-12-11	Exact identifier application number: M020
Lip Protection	TITANIUM DIOXIDE, ZINC OXIDE	Teton Dermatology Holdings, Inc.	3509eea7-f966-2080-e063-6294a90aeeb5	2025-12-11	Exact identifier application number: M020
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	HALEM DERMATOLOGY PLLC	35bce44e-d9f4-9279-e063-6394a90a6453	2025-12-11	Exact identifier application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
62032-140-05	62032014005	28 g in 1 TUBE	28 g				Historical
62032-690-02	62032069002	1 BAG in 1 CARTON (62032-690-02) / 1 KIT in 1 BAG * 1 BOTTLE, DROPPER in 1 CARTON / 30 mL in 1 BOTTLE, DROPPER * 1 BOTTLE, PUMP in 1 CARTON / 48 g in 1 BOTTLE, PUMP * 28 g in 1 TUBE (62032-140-05)	1 bag	2023-03-20	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
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