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 162 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pipette Diaper Rash ZINC OXIDE Pipette LLC 2a93998c-1855-9207-e063-6294a90ab0e9 2025-11-14 Warnings Exact identifier application number: M020 Ware Sonny Universal TITANIUM DIOXIDE, ZINC OXIDE Ware Cosmetics fe2b9d16-9215-e21e-e053-6394a90a5156 2025-11-14 Warnings Exact identifier application number: M020 YAY NOVELTY ALL-IN-ONE TITANIUM DIOXIDE, ZINC OXIDE YAY Novelty fb833158-d0d8-de7f-e053-6294a90adc5a 2025-11-14 Warnings Exact identifier application number: M020 Thu Brule Free Spirit Correct and Protect TITANIUM DIOXIDE, ZINC OXIDE Laughing Buddha LLC 258a4f97-d811-0521-e063-6394a90aaf3b 2025-11-14 Warnings Exact identifier application number: M020 Alpha-H Total Eclipse TITANIUM DIOXIDE, ZINC OXIDE Alpha-H fc8a4efe-7d5e-5f44-e053-6394a90a80aa 2025-11-14 Warnings Exact identifier application number: M020 Svens Everyday Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Svens, Inc 912170ae-124c-5eb9-e053-2995a90a0ba3 2025-11-14 Warnings Exact identifier application number: M020 Wander Beauty Pack Up and Glow Priming TITANIUM DIOXIDE, ZINC OXIDE Wander Beauty 3d844efc-091c-9a9b-e063-6294a90aee7c 2025-11-14 Warnings Exact identifier application number: M020 Baby Bare Republic Mineral Sunscreen ZINC OXIDE COOLA, LLC b292d1a9-7ff8-0faf-e053-2995a90ae342 2025-11-14 Warnings Exact identifier application number: M020 Aspen Islanders Sheer Mineral Sport ZINC OXIDE Aspen Islanders LLC 0fcb2adf-71c9-3369-e063-6294a90aa806 2025-11-14 Warnings Exact identifier application number: M020 By the Beach Suncare SPF 30 SUNCARE MALON DAZE By the Beach Suncare LLC 4391728b-dfe7-3ffb-e063-6394a90a240e 2025-11-14 Warnings Exact identifier application number: M020 By the Beach Suncare SPF 30 SUNCARE CITRUS CRUSH By the Beach Suncare LLC 43918d25-e947-5e17-e063-6394a90ada7c 2025-11-14 Warnings Exact identifier application number: M020 By the Beach Suncare SPF 30 SUNCARE CANDY CLOUDS By the Beach Suncare LLC 4391728b-dfe8-3ffb-e063-6394a90a240e 2025-11-14 Warnings Exact identifier application number: M020 Sunsolve MD Balance and Clear ZINC OXIDE Sunsolve MD Inc 26f3595d-adef-a8a5-e063-6394a90adfd4 2025-11-14 Warnings Exact identifier application number: M020 Sunsolve MD Detox and Shield ZINC OXIDE Sunsolve MD Inc 26f3886b-a3a5-c9b7-e063-6394a90af6c3 2025-11-14 Warnings Exact identifier application number: M020 Sunsolve MD Mineral Shade Amber 002 ZINC OXIDE Sunsolve MD Inc 26e00001-9c68-0734-e063-6394a90a1787 2025-11-14 Warnings Exact identifier application number: M020 Sunsolve MD Mineral Shade Agate 003 ZINC OXIDE Sunsolve MD Inc 26e00001-9c6f-0734-e063-6394a90a1787 2025-11-14 Warnings Exact identifier application number: M020 Sunsolve MD Mineral Shade Bronzite 004 ZINC OXIDE Sunsolve MD Inc 26e13356-9ab5-246a-e063-6394a90a2a70 2025-11-14 Warnings Exact identifier application number: M020 Sunsolve MD Mineral Shade Onyx 006 ZINC OXIDE Sunsolve MD Inc 26e16b5e-dd2e-6fb8-e063-6394a90a6a7f 2025-11-14 Warnings Exact identifier application number: M020 Sunsolve MD Calm and Revitalize ZINC OXIDE Sunsolve MD Inc 26f3f534-a305-3530-e063-6394a90a75e1 2025-11-14 Warnings Exact identifier application number: M020 Sunsolve MD Mineral Shade Garnet 005 ZINC OXIDE Sunsolve MD Inc 26e1508f-d386-329b-e063-6394a90a0a98 2025-11-14 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