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 193 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sun Bum Kids 50 Clear Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	3c1f619e-dd4e-ab62-e063-6294a90a10d4	2025-08-22	Warnings	Exact identifier application number: M020
Sun Bum Premium Moisturizing Sunscreen Broad Spectrum SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	3cf8c55b-5203-3a96-e063-6294a90a4e9e	2025-08-22	Warnings	Exact identifier application number: M020
Baby Bum Mineral 50 Sunscreen	ZINC OXIDE	Sun Bum LLC	369f449f-fb9d-5529-e063-6394a90ac3b2	2025-08-22	Warnings	Exact identifier application number: M020
PHOFAY Matte Sunscreen Liquid Foundation SPF 30 4	ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE	Longway Technology(Guangzhou) Co., Ltd.	3cdc1ae9-2924-5057-e063-6294a90ad2f3	2025-08-21	Warnings	Exact identifier application number: M020
PHOFAY Matte Sunscreen Liquid Foundation SPF 30 3	ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE	Longway Technology(Guangzhou) Co., Ltd.	3b21f1d8-534d-f4ea-e063-6294a90ad2eb	2025-08-21	Warnings	Exact identifier application number: M020
LBEL CONCENTRE GLOBAL ANTI AGING SERUM FOUNDATION SPF 15 ALMENDRA 230N	OCTINOXATE, ZINC OXIDE	BEL STAR S.A.	2cb3cd01-8871-59a0-e063-6394a90ac0f7	2025-08-21	Warnings	Exact identifier application number: M020
Neutrogena Triple Age Repair Moisturizer with Sunscreen Broad Spectrum SPF 25	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Kenvue Brands LLC	a6011835-cd2f-476f-9ec1-721f896483c5	2025-08-21	Warnings	Exact identifier application number: M020
Neutrogena Beach Defense Water Plus Sun Protection Sunscreen Broad Spectrum SPF30	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Kenvue Brands LLC	35fc2571-370c-42aa-986c-b1fa58658d86	2025-08-21	Warnings	Exact identifier application number: M020
Sun Bum 50 Sunscreen Face Stick	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	3ce436e8-bc22-b9d7-e063-6394a90a57c4	2025-08-21	Warnings	Exact identifier application number: M020
CYZONE CY PLAY CREAMY LIP BALM HIDRATANTE EN BARRA PARA LABIOS 24H FPS 12 FUCHSIA CREAMY	OCTINOXATE, ZINC OXIDE	BEL STAR S A	ea39a1c0-6b12-77ba-e053-2995a90a7314	2025-08-21	Warnings	Exact identifier application number: M020
Neutrogena Clear Face Breakout Free Oil Free Sunscreen Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Kenvue Brands LLC	cd211d06-b91e-44b1-99fe-fa0794f10221	2025-08-21	Warnings	Exact identifier application number: M020
Sun Bum Sunscreen Lip Balm Broad Spectrum SPF 30 Kiwi	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	3cd51497-693e-bf79-e063-6394a90a5e48	2025-08-21	Warnings	Exact identifier application number: M020
LBEL SOLUTIONS PRO-NUDE SKIN ULTRA-LIGHT SERUM FOUNDATION WITH NIACINAMIDE SPF 20 CHAMPAGNE 170N	OCTINOXATE, ZINC OXIDE	BEL STAR S.A.	2f769ed5-0176-8c80-e063-6394a90a92c6	2025-08-21	Warnings	Exact identifier application number: M020
Sun Bum 30 Premium Moisturizing Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	21caf385-f11b-146a-e063-6294a90aa851	2025-08-21	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	3ce6d119-5e3e-dfa4-e063-6394a90a474b	2025-08-21	Warnings	Exact identifier application number: M020
Sun Bum 50 Premium Moisturizing Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	21cb8652-c6d0-0a77-e063-6294a90a6e1e	2025-08-21	Warnings	Exact identifier application number: M020
Sun Bum Signature High Performance Mineral Sunscreen Face Stick 30	ZINC OXIDE	Sun Bum, LLC	3ce81478-196e-d87b-e063-6294a90afd58	2025-08-21	Warnings	Exact identifier application number: M020
Premium Moisturizing Sunscreen Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	33164cea-e31e-9fcc-e063-6294a90a307e	2025-08-21	Warnings	Exact identifier application number: M020
PHOFAY Matte Sunscreen Liquid Foundation SPF 30 5	ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE	Longway Technology(Guangzhou) Co., Ltd.	3ceb3368-439c-9f6c-e063-6294a90a98ba	2025-08-21	Warnings	Exact identifier application number: M020
PHOFAY Matte Sunscreen Liquid Foundation SPF 30 2	ENSULIZOLE ,HOMOSALATE ,OCTINOXATE,TITANIUM DIOXIDE	Longway Technology(Guangzhou) Co., Ltd.	3cc8b151-c07d-7473-e063-6294a90a1cc7	2025-08-20	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