Home NDC 62032-690 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.
FDA-Initiated Inactive NDC Indexing# 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 114 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Kind Restore Tinted Mineral Sunscreen ZINC OXIDE POLISH BEAUTY 3980d278-c0f4-2c59-e063-6394a90aac37 2025-12-16 Exact identifier application number: M020 Solar Eclipse Extreme Sunscreen ZINC OXIDE ULTRAVIOLET SKINCARE LLC 36bfa691-48c0-8033-e063-6294a90ad899 2025-12-16 Exact identifier application number: M020 Kind Restore Moisturizing Lip Balm TITANIUM DIOXIDE, ZINC OXIDE POLISH BEAUTY 39814e27-4f3f-5ee6-e063-6394a90a941b 2025-12-16 Exact identifier application number: M020 Yoali SPF 40 ZINC OXIDE YOALI STUDIO LLC 390b7f9c-bc04-80ec-e063-6294a90a4092 2025-12-16 Exact identifier application number: M020 Skin Defense Matte Tinted Sunscreen ZINC OXIDE Gentlehomme LLC 365eb727-3e7f-f1dd-e063-6394a90aa469 2025-12-16 Exact identifier application number: M020 Dr B Clinical Skin Care Tinted Sunscreen TITANIUM DIOXIDE, ZINC OXIDE NAIRA BABAIAN, M.D., P.A. 365da1f8-5250-7589-e063-6294a90a3e68 2025-12-16 Exact identifier application number: M020 Dr B Clinical Skin Care Non Tinted Sunscreen TITANIUM DIOXIDE, ZINC OXIDE NAIRA BABAIAN, M.D., P.A. 365d7564-3025-257b-e063-6294a90ad170 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen ZINC OXIDE Gentlehomme LLC 365e7d8e-e3e0-4c08-e063-6294a90af415 2025-12-16 Exact identifier application number: M020 Daily Replenish mineral sunscreen ZINC OXIDE PURE VITALITY SKIN AND BODY, INC 369896b1-f4b4-6201-e063-6394a90a5bca 2025-12-16 Exact identifier application number: M020 Zinc 20 mineral sunscreen face Plus body ZINC OXIDE PURE VITALITY SKIN AND BODY, INC 36985373-22dd-2232-e063-6394a90a76fb 2025-12-16 Exact identifier application number: M020 Matte Defense Mineral Sunscreen non tinted TITANIUM DIOXIDE, ZINC OXIDE PURE VITALITY SKIN AND BODY, INC 3698090a-1639-00f9-e063-6394a90a7dd1 2025-12-16 Exact identifier application number: M020 Daily Replenish mineral sunscreen ZINC OXIDE PURE VITALITY SKIN AND BODY, INC 3698d309-b9bf-e197-e063-6294a90af5a1 2025-12-16 Exact identifier application number: M020 Zinc 20 mineral sunscreen face Plus body ZINC OXIDE PURE VITALITY SKIN AND BODY, INC 3698f29e-5d80-94af-e063-6394a90a0489 2025-12-16 Exact identifier application number: M020 Tinted Mineral Primer SPF 40 TITANIUM DIOXIDE, ZINC OXIDE JOSEPHINA RAMIREZ 365cf2be-8862-3622-e063-6394a90ac4e3 2025-12-16 Exact identifier application number: M020 SANCTUARY Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE CHAMPAGNE APOTHECARY LLC 365ca99c-c878-1f4b-e063-6394a90a1f53 2025-12-16 Exact identifier application number: M020 Tinted Mineral Defense SPF 40 ZINC OXIDE JOSEPHINA RAMIREZ 365d299a-5886-5597-e063-6394a90a336c 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE MILL VALLEY DERMATOLOGY, INC. 3b171a89-c757-47a1-e063-6294a90a7a64 2025-12-16 Warnings Exact identifier application number: M020 Tinted BB Cream ZINC OXIDE Eco Esthetics LLC 38f3e618-59e1-4504-e063-6394a90afa55 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen ZINC OXIDE MADRE TIERRA, INC. 3f697463-d3db-7b73-e063-6394a90ac222 2025-12-16 Warnings Exact identifier application number: M020 Non-Tinted Replenishing Daily Protection ZINC OXIDE MADRE TIERRA, INC. 3f69d6f3-454b-e60a-e063-6394a90a8781 2025-12-16 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