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 35 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
THANKYOU FARMER Sun Project Soothing Sun	OCTISALATE, OCTINOXATE, OCTOCRYLENE, AVOBENZONE, HOMOSALATE	THANK YOU FARMER CO., LTD	300ab1bc-9c11-c2f0-e063-6394a90aa853	2026-05-06	Warnings	Exact identifier application number: M020
Sheer Defense Tinted Broad Spectrum Sunscreen SPF 50	ZINC OXIDE, OCTINOXATE	Private Label Skin Care	9eb7f287-cb61-4f9d-968e-16b195dbbc9a	2026-05-06	Warnings	Exact identifier application number: M020
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 1W Warm	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	53a79ee7-312b-49a2-8a9b-c50794fcd171	2026-05-05	Warnings	Exact identifier application number: M020
SPF 50 Dry Tropix with fragrance	HOMOSALATE 10.00% OCTISALATE 5.00% AVOBENZONE 3.00%	Surface Products Corp	2c95f5c0-7ff6-4eac-b2d6-49e7da7e7bec	2026-05-05	Warnings	Exact identifier application number: M020
SURFACE SUN SPF30 DRY TOUCH Fragrance Free	HOMOSALATE 10.00% OCTOCRYLENE 6.00% AVOBENZONE 3.00%	Surface Products Corp	9592835a-7c07-487e-a955-04fdea070809	2026-05-05	Warnings	Exact identifier application number: M020
SURFACE SUN SPF 50 DRY TOUCH Fragrance Free	HOMOSALATE 10.00% OCTOCRYLENE 6.00% AVOBENZONE 3.00%	Surface Products Corp	65f52fc8-8ddb-4282-9bc0-92a7d0e0c0f2	2026-05-05	Warnings	Exact identifier application number: M020
Knesko Skin The Sunscreen	ZINC OXIDE	Knesko, LLC	5114dc75-a865-326e-e063-6294a90a8911	2026-05-05	Warnings	Exact identifier application number: M020
SURFACE SUN SPF 50 DRY TOUCH Fragrance Free	HOMOSALATE 10.00% OCTOCRYLENE 6.00% AVOBENZONE 3.00%	Surface Products Corp	683cb489-e4e1-44ab-9543-614d42b08edd	2026-05-05	Warnings	Exact identifier application number: M020
Neutrogena MINERAL UV TINT FACE DEEP SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Port Jervis Laboratories, Inc	51169bed-2091-ad2b-e063-6294a90a84b6	2026-05-05	Warnings	Exact identifier application number: M020
Surface Sun SPF 50 Mineral Sunscreen	ZINC OXIDE 24%	Surface Products Corp	6f95de43-cb71-4ddd-b438-a35ee2e14fae	2026-05-05	Warnings	Exact identifier application number: M020
Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 70	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Port Jervis Laboratories, Inc	5118a0a4-728b-6884-e063-6394a90a02b3	2026-05-05	Warnings	Exact identifier application number: M020
Carmex Daily Care Moisturizing Lip Balm Strawberry SPF 15	OCTINOXATE, OXYBENZONE	Carma Laboratories, Inc.	baed7205-2e0d-c6aa-e053-2995a90a8e29	2026-05-05	Warnings	Exact identifier application number: M020
Carmex Daily Care Moisturizing Lip Balm Strawberry SPF 15	OCTINOXATE, OXYBENZONE	Carma Laboratories, Inc.	baee366f-c1a0-5e21-e053-2a95a90a6687	2026-05-05	Warnings	Exact identifier application number: M020
Carmex Sun and Soothe Moisturizing Lip Balm SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Carma Laboratories, Inc.	fc4d2387-ce6a-4105-bab4-7d371b61f770	2026-05-05	Warnings	Exact identifier application number: M020
THANKYOU FARMER Sun Project Soothing Sun	HOMOSALATE, OCTISALATE. AVOBENZONE	THANK YOU FARMER CO., LTD	3009df84-4ca7-e170-e063-6294a90a1578	2026-05-05	Warnings	Exact identifier application number: M020
THANKYOU FARMER Sun Project Moisture Sun	HOMOSALATE, OCTOCRYLENE, OCTISALATE, OCTINOXATE, AVOBENZONE	THANK YOU FARMER CO., LTD	300d8526-0daf-2255-e063-6394a90a21b1	2026-05-05	Warnings	Exact identifier application number: M020
LUMINOUS EYE CORRECTOR SPF 41 - FAIR	TITANIUM DIOXIDE, ZINC OXIDE	Drmtlgy, LLC	8cfb1f8c-1bd7-4983-ab82-1c9bd8925afa	2026-05-04	Warnings	Exact identifier application number: M020
LUMINOUS EYE CORRECTOR SPF 41 - DEEP	TITANIUM DIOXIDE, ZINC OXIDE	Drmtlgy, LLC	930bd1de-5a0e-4607-8d3c-b1ca918f890b	2026-05-04	Warnings	Exact identifier application number: M020
THANKYOU FARMER Sun Project Rice Tinted Mineral Sunscreen	ZINC OXIDE	THANK YOU FARMER CO., LTD	30086b1e-d876-2528-e063-6294a90a4e9f	2026-05-04	Warnings	Exact identifier application number: M020
Blue Berry SPF 15 Broad Spectrum Lip Balm	BLUE BERRY SPF 15 BROAD SPECTRUM LIP BALM	Raining Rose, Inc	50ff6ecb-c8b3-02fc-e063-6394a90a68de	2026-05-04	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