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 157 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join EcoZinc Natural Mineral Sunscreen SPF50 ZINC OXIDE SUNSCREEN VEGANIC SKN LIMITED 386e23ec-7618-f42c-e063-6394a90a595d 2025-11-27 Warnings Exact identifier application number: M020 KOVR Military grade sunscreen for Men ZINC OXIDE ACTIVE LIFE INC c9fbbc6e-6284-4308-89a3-98300c3a0320 2025-11-26 Warnings Exact identifier application number: M020 Alba Botanica Sensitive Mineral SPF 50 ZINC OXIDE The Hain Celestial Group, Inc. 4484b16f-f29a-60cc-e063-6294a90a2b9d 2025-11-26 Warnings Exact identifier application number: M020 Alba Botanica Sheer Mineral SPF50 ZINC OXIDE The Hain Celestial Group, Inc. 0cf9c4b9-8e85-980c-e063-6394a90a9e7e 2025-11-26 Warnings Exact identifier application number: M020 Alba Botanica Sensitive Mineral SPF 30 ZINC OXIDE The Hain Celestial Group, Inc. 44867882-d9c1-7389-e063-6294a90a7f77 2025-11-26 Warnings Exact identifier application number: M020 Alba Botanica Sheer Mineral SPF30 ZINC OXIDE The Hain Celestial Group, Inc. 0cf9361f-f292-6429-e063-6294a90add0e 2025-11-26 Warnings Exact identifier application number: M020 ZO Skin Health Gel Sunscreen Broad-Spectrum SPF 50 AVOBENZONE, OCTISALATE, OCTOCRYLENE ZO Skin Health, Inc. ec8386f2-9cb7-40f4-e053-2995a90ac2d8 2025-11-26 Warnings Exact identifier application number: M020 WOODSLEEP Tallow Sunscreen TITANIUM DIOXIDE Shantou Woodsleep Biotechnology Co., Ltd. 330a9f2e-7ce1-f83f-e063-6394a90a184a 2025-11-26 Warnings Exact identifier application number: M020 WOODSLEEP Tallow Sunscreen TITANIUM DIOXIDE Shantou Woodsleep Biotechnology Co., Ltd. 33cdde09-e7ee-e003-e063-6394a90a8762 2025-11-26 Warnings Exact identifier application number: M020 Native Mineral Suncare Zinc Oxide Sunscreen Tropical Breeze Broad Spectrum SPF 30 ZINC OXIDE The Procter & Gamble Manufacturing Company 44718c3c-b081-bcfb-e063-6394a90a3786 2025-11-25 Warnings Exact identifier application number: M020 Native Mineral Suncare Zinc Oxide Sunscreen Unscented Broad Spectrum SPF 30 ZINC OXIDE The Procter & Gamble Manufacturing Company 4472cc1e-6b34-388b-e063-6394a90ac7b6 2025-11-25 Warnings Exact identifier application number: M020 Native Mineral Suncare Zinc Oxide Sunscreen Pear and Coconut Water Broad Spectrum SPF 30 ZINC OXIDE The Procter & Gamble Manufacturing Company 4472ef69-8992-fcab-e063-6294a90a6b90 2025-11-25 Warnings Exact identifier application number: M020 Native Mineral Suncare Zinc Oxide Sunscreen Vanilla Milk and Shea Broad Spectrum SPF 30 ZINC OXIDE The Procter & Gamble Manufacturing Company 44732f89-8ac3-8c5d-e063-6394a90aba73 2025-11-25 Warnings Exact identifier application number: M020 Native Mineral Suncare Zinc Oxide Sunscreen Unscented Broad Spectrum SPF 30 ZINC OXIDE The Procter & Gamble Manufacturing Company 447347d6-b8a3-7338-e063-6294a90abbf9 2025-11-25 Warnings Exact identifier application number: M020 Native Mineral Suncare Zinc Oxide Sunscreen Pear and Coconut Water Broad Spectrum SPF 30 ZINC OXIDE The Procter & Gamble Manufacturing Company 4473c4cc-f8b5-4a92-e063-6394a90ae690 2025-11-25 Warnings Exact identifier application number: M020 salmon colored sunscreen SALMON COLORED SUNSCREEN Guangzhou Fantesy Biotechnology Co.,Ltd 4477964b-28f3-a371-e063-6294a90a4230 2025-11-25 Warnings Exact identifier application number: M020 Safe Sea SPF 50 Mineral ZINC OXIDE Nidaria Technology Ltd. f6cf9454-552b-486e-a38b-ab3c183b24a1 2025-11-24 Warnings Exact identifier application number: M020 Safe Sea SPF 30 ZINC OXIDE Nidaria Technology Ltd. 91bf07ed-0be4-43c9-b5f3-4e8eb892bca5 2025-11-24 Warnings Exact identifier application number: M020 Olay Complete UV365 Daily Moisturizer Sensitive Broad Spectrum SPF 15 OCTINOXATE AND ZINC OXIDE The Procter & Gamble Manufacturing Company 5904baa8-3070-1d77-e053-2a91aa0a6852 2025-11-24 Warnings Exact identifier application number: M020 it cosmetics Bye Bye Foundation Full Coverage Moisturizer with 3D Skin Flex Broad Spectrum SPF 50 Plus UVA UVB Physical Sunscreen All Shades TITANIUM DIOXIDE AND ZINC OXIDE L'Oreal USA, Inc. 86eea4df-4191-4e05-9f05-4a98ef8c2a4d 2025-11-24 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