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 250 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens SPF 50 Hydrating	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	f347588d-8225-45a7-e053-2995a90ab688	2024-12-22	Warnings	Exact identifier application number: M020
Mineral Sunstick	ZINC SPF STICK	Tubby Todd	29e41fe8-4e17-dbaa-e063-6294a90a4a10	2024-12-22	Warnings	Exact identifier application number: M020
Mineral Sunscreen	ZINC OXIDE SPF 50	Tubby Todd	29e487da-5312-8192-e063-6294a90ad809	2024-12-22	Warnings	Exact identifier application number: M020
EcoStick Sunscreen SPF 35	ZINC OXIDE, TITANIUM DIOXIDE	Stream2Sea, LLC	eba17b7a-5e96-4462-9b71-44c2bc577dce	2024-12-21	Warnings	Exact identifier application number: M020
Planet Protecting Sunscreen 30	TITANIUM DIOXIDE	Stream2Sea, LLC	89e44c5f-121e-4fdd-b9e0-023909ea32f5	2024-12-21	Warnings	Exact identifier application number: M020
BABYGANICS SPF 50 Plus SUNSCREEN	ZINC OXIDE, OCTISALATE, AND OCTOCRYLENE	KAS Direct LLC dba Babyganics	4075f9dc-c25f-434f-a3fc-a7f896295c3d	2024-12-20	Warnings	Exact identifier application number: M020
Sunscreen	HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE	Total Resources International	7d4f820d-e154-428e-89c2-2e26e088ceef	2024-12-20	Warnings	Exact identifier application number: M020
Babyganics Sheer Blend SPF50 Mineral Sunscreen	ZINC OXIDE	KAS Direct LLC dba BabyGanics	edced0dc-dd43-4ac9-b816-f4edb45fc87b	2024-12-20	Warnings	Exact identifier application number: M020
NARS Radiance Primer Broad Spectrum SPF 35 Sunscreen	OCTISALATE, OCTOCRYLENE, AVOBENZONE, HOMOSALATE	COSMAX USA, CORPORATION	29ad7391-d932-3549-e063-6394a90ab2b2	2024-12-20	Warnings	Exact identifier application number: M020
Face Reality daily spf 30 plus Sunscreen SPF 30	HOMOSALATE, OCTISALATE, AVOBENZONE	Face Reality,LLC	45a3ce12-15fe-4040-95da-ac8513a39fb9	2024-12-20	Warnings	Exact identifier application number: M020
Face Reality mineral matte spf 28 Sunscreen SPF 28	ZINC OXIDE, TITANIUM DIOXIDE	Face Reality, LLC	29b70afe-cf9d-d0ba-e063-6394a90a1cc4	2024-12-20	Warnings	Exact identifier application number: M020
Sonage Roux Tinted Day Creme with SPF 30 Sheer Tinted Moisturizer	ZINC OXIDE	ASA Universal Inc. dba: Sonage	fd14d70c-6cd0-5de6-e053-6294a90a7add	2024-12-20	Warnings	Exact identifier application number: M020
Coola SPF 50 Classic	SUNSCREEN FACE MIST	COOLA LLC	d18d0dac-5690-436e-e053-2995a90a0254	2024-12-20	Warnings	Exact identifier application number: M020
COOLA Mineral Body SPF 30 Tropical Coconut	ZINC OXIDE	COOLA, LLC	eeb5d4f1-8cba-9ef6-e053-2a95a90a823f	2024-12-20	Warnings	Exact identifier application number: M020
Oars and Alps SPF 50 100% Mineral Antioxidant Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Oars and Alps LLC	f3971b85-a13e-4195-e053-2995a90a73cb	2024-12-20	Warnings	Exact identifier application number: M020
Vacation SPF 30 Mineral	ZINC OXIDE	Vacation Inc.	f69513ae-f210-075f-e053-2a95a90a9b2e	2024-12-20	Warnings	Exact identifier application number: M020
Vacation SPF 30 Chardonnay Oil	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Vacation Inc.	f694752d-4839-3768-e053-2995a90a5d3e	2024-12-20	Warnings	Exact identifier application number: M020
Oars and Alps SPF 50 Hydrating Antioxidant SunscreenSpray	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Oars and Alps LLC	ec5b82f5-b36c-fbc5-e053-2995a90afa0c	2024-12-20	Warnings	Exact identifier application number: M020
Oars and Alps SPF 70 Hydrating Antioxidant Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Oars and Alps LLC	f39673a7-0b62-bdf7-e053-2995a90aa2b7	2024-12-20	Warnings	Exact identifier application number: M020
Carpe SPF 30 Face Primer	TITANIUM DIOXIDE, ZINC OXIDE	Clutch, Inc. DBA Carpe	feac5ee2-faa5-fd17-e053-6394a90a7f99	2024-12-20	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