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 22 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Unseen Sunscreen SPF 50	OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE	Supergoop LLC	21b3491f-7b02-9bc5-e063-6294a90a0dc3	2026-06-04	Warnings	Exact identifier application number: M020
Mineral Glowscreen Soft-Radiance Drops Golden Hour	ZINC OXIDE	Supergoop LLC	1f1be2a7-af96-d73d-e063-6394a90acc1a	2026-06-04	Warnings	Exact identifier application number: M020
Play Antioxidant Body Mist WIth Vitamin C Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	975402e6-8c74-b18e-e053-2995a90a467e	2026-06-04	Warnings	Exact identifier application number: M020
Derma E Sun Drops SPF 30	ZINC OXIDE	derma e	76c29f24-e0d9-4235-b278-96e609bc58db	2026-06-04	Warnings	Exact identifier application number: M020
ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB	ZINC OXIDE OCTOCRYLENE ETHYLHEXYL SALICYLATE HOMOSALATE TITANIUM DIOXIDE	HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED	5354af18-50c4-5fba-e063-6394a90ace39	2026-06-03	Warnings	Exact identifier application number: M020
ATOMY BB SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	ATOMY CO., LTD.	b0cd27ee-4917-4800-bcdf-c6e14b28c1d1	2026-06-02	Warnings	Exact identifier application number: M020
Atomy Sunscreen White Broad Spectrum SPF 50 PLUS	HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	ATOMY CO., LTD.	ad0b9091-a990-45bf-93f4-d886be1bbffe	2026-06-02	Warnings	Exact identifier application number: M020
Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS	HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	ATOMY CO., LTD.	994d5680-284e-4faf-a29b-4d28f8d46e8f	2026-06-02	Warnings	Exact identifier application number: M020
BLDG Active Skin Repair Sun Stick Performance Sunscreen	ZINC OXIDE	Innovacyn, Inc.	a751fc1d-5ee4-4ecc-8ade-2568d91890c4	2026-06-02	Warnings	Exact identifier application number: M020
ANESSA PERFECT UV SUNSCREEN SKINCARE	HOMOSALATE OCTOCRYLENE ETHYLHEXYL SALICYLATE	HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED	5347c9a1-2239-b617-e063-6294a90ac601	2026-06-02	Warnings	Exact identifier application number: M020
Sungboon Editor Hydro Booster Moisture Sunscreen	HOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE	Olive International Co., Ltd.	4ea2292a-571c-475c-a64c-cbdd1f51f242	2026-06-02	Warnings	Exact identifier application number: M020
Sungboon Editor Daily Invisible Blurring Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Olive International Inc.	42325963-0917-43c4-8fe0-130336c7fa81	2026-06-02	Warnings	Exact identifier application number: M020
Matte Veil Tinted Broad Spectrum Sunscreen SPF 40	ZINC OXIDE, TITANIUM DIOXIDE	Private Label Skin Care	a8d60212-18a7-42af-8bb3-bfcff7690a49	2026-06-02	Warnings	Exact identifier application number: M020
The Mineral Melt SPF30	ZINC OXIDE, TITANIUM DIOXIDE	Dune Suncare Inc.	2114fc3b-c8ce-45d2-8a82-4dc54f0adaf3	2026-06-02	Warnings	Exact identifier application number: M020
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS UV AIR MINERAL SERUM SUNSCREEN BROAD SPECTRUM SPF 50	TITANIUM DIOXIDE AND ZINC OXIDE	LOreal USA Products Inc	a1acb789-5bf4-4447-b3c5-4a7d4d3013a7	2026-06-01	Warnings	Exact identifier application number: M020
4ocean REEF SAFE SUNSCREEN SPF 40	ZINC OXIDE	Stream2Sea, LLC	52d3d97c-a846-4721-acbe-52a525cb2011	2026-06-01	Warnings	Exact identifier application number: M020
APRILSKIN MUGWORT CALMING SUNSCREEN	OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE	APR US INC	50a7b64a-8b26-97ac-e063-6294a90ad77a	2026-06-01	Warnings	Exact identifier application number: M020
Ultra Violette Future Screen Broad Spectrum SPF 50	ZINC OXIDE	Grace and Fire USA Inc.	252fdc91-bbe2-58ec-e063-6294a90a5067	2026-06-01	Warnings	Exact identifier application number: M020
Ultra Violette Vibrant Screen Broad Spectrum SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Grace and Fire USA Inc.	2633a289-b3b2-b614-e063-6294a90ad214	2026-06-01	Warnings	Exact identifier application number: M020
Ultra Violette Sequin Supreme SPF 50	OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE	Grace and Fire USA Inc.	41027faa-7d61-4970-e063-6294a90a7df4	2026-06-01	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