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 14 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
UV RESTORE FACE SERUM SUNSCREEN SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	COSMAX USA	564b8070-ee59-0c24-e063-6294a90ad9a9	2026-07-10	Warnings	Exact identifier application number: M020
COCO-EVE COCONUT MILK BODY SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	COSMAX USA	564b80c2-16e0-fb5f-e063-6394a90a50d2	2026-07-10	Warnings	Exact identifier application number: M020
COCO EVE SUNNY HONEY HIGHLIGHTER BODY SPF 50	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	COSMAX USA	564b9b1f-3d5b-4349-e063-6294a90a3b77	2026-07-10	Warnings	Exact identifier application number: M020
NORWEX Lip Glaze Broad Spectrum SPF 30 Hazelnut	ZINC OXIDE	COSMAX USA	564ba912-c44b-4940-e063-6294a90a28fa	2026-07-10	Warnings	Exact identifier application number: M020
MISTINE UV INVISIBLE FACE SHEER SUNSCREEN SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	COSMAX USA	564bbb5f-4000-390d-e063-6294a90a408d	2026-07-10	Warnings	Exact identifier application number: M020
PEACH AND LILY SUN COVER MINERAL SUNSCREEN SPF 30	ZINC OXIDE	COSMAX USA	564bb5f9-5ac5-548b-e063-6394a90a8462	2026-07-10	Warnings	Exact identifier application number: M020
ILLUSION LUMINOUS GLOW FOUNDATION	AVOBENZONE, HOMOSALATE, AND OCTISALATE	Kingdom Animalia, LLC DBA Hourglass Cosmetics	cf6a7e1a-7bca-439c-808a-80262f095f84	2026-07-10	Warnings	Exact identifier application number: M020
Tula Skincare Protect and Glow Daily Facial Sunscreen Gel SPF 30	AVOBENZONE, HOMOSALATE, AND OCTISALATE	The Procter & Gamble Manufacturing Company	30a063fa-e537-a2c1-e063-6394a90a6a83	2026-07-09	Warnings	Exact identifier application number: M020
Olay Complete Lightweight with Sunscreen Broad Spectrum SPF 15 Sensitive	OCTINOXATE AND ZINC OXIDE	The Procter & Gamble Manufacturing Company	3cb971e1-34f1-ee89-e063-6394a90a52a9	2026-07-09	Warnings	Exact identifier application number: M020
Olay Complete Lightweight with Sunscreen Broad Spectrum SPF 30 Sensitive	OCTINOXATE, OCTISALATE, OCTOCRYLENE, AND ZINC OXIDE	The Procter & Gamble Manufacturing Company	3cb9de81-f05e-9697-e063-6394a90a69c5	2026-07-09	Warnings	Exact identifier application number: M020
Bombee Honey Daily Glow Shield Sunscreen	HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE	ABT ASIA Inc.	56112dff-b091-7a56-e063-6294a90a77d3	2026-07-08	Warnings	Exact identifier application number: M020
Sunny C Sunscreen SPF 50	SUNNY C SUNSCREEN	MIXIK, INC.	4ed2a482-6c63-69f5-e063-6394a90ad3ee	2026-07-08	Warnings	Exact identifier application number: M020
Ultra Violette Supreme Screen Broad Spectrum SPF 50	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Grace and Fire USA Inc.	24389324-19db-7eb5-e063-6394a90ad7fb	2026-07-08	Warnings	Exact identifier application number: M020
ANEW ULTIMATE DAY MULTI-PERFORMANCECREAM SPF 25 SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTINOXATE,OXYBENZONE	COSMAX USA, CORPORATION	562053d4-12bd-976e-e063-6394a90a59de	2026-07-08	Warnings	Exact identifier application number: M020
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	DERMIO DERMATOLOGY LLC	562f5b0d-6a10-305d-e063-6394a90a5980	2026-07-08	Warnings	Exact identifier application number: M020
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	Suzanne's Skin2soul LLC	562fbaa6-f93a-5ec4-e063-6294a90a9634	2026-07-08	Warnings	Exact identifier application number: M020
Sun Protection Mineral SPF 30	ZINC OXIDE	derma e	bf6474a7-a21f-49cb-86e6-e5c40dbd34c3	2026-07-08	Warnings	Exact identifier application number: M020
Aussie Betta Tallow Sunscreen SPF50 SPF50	TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREEN	AUSSIE BETTA HEALTHY CARE PTY LTD	56007d82-ff5b-6c26-e063-6294a90a09b6	2026-07-07	Warnings	Exact identifier application number: M020
Bath and Body Works SPF Pink Dream	AVOBENZONE,HOMOSALATE,OCTISALATE	Bath & Body Works, Inc.	560785f5-9126-12ba-e063-6294a90ac946	2026-07-07	Warnings	Exact identifier application number: M020
Bath and Body Works SPF Sunkissed Berry	AVOBENZONE,HOMOSALATE,OCTISALATE	Bath & Body Works, Inc.	56078698-8655-12bd-e063-6294a90ad34c	2026-07-07	Warnings	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