Home NDC 62032-140 SUN SHIELD BROAD SPECTRUM SPF 50 MATTE
Product NDC 62032-140
11-digit product format 620320140
Labeler code 62032
Product ID 62032-140_7415289e-2b1a-416a-ab5d-2fafa7059e17
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE, and ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler Obagi Cosmeceuticals LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-15
Substance HOMOSALATE; OCTISALATE; ZINC OXIDE
Active strength 100; 50; 165 mg/g; mg/g; mg/g
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 · 32 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 2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 62032-140-34 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 62032-140-05 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 62032-140-09 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…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 62032-140-34 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 62032-140-05 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 62032-140-09 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 62032-140-34 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 62032-140-05 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 62032-140-09 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 62032-140-34 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 62032-140-05 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 62032-140-09 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 62032-140-34 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 62032-140-05 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 62032-140-09 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 62032-140-34 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 62032-140-09 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 62032-140-05 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 62032-140-34 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 62032-140-09 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 62032-140-05 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 62032-140-34 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 62032-140-09 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 62032-140-05 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 SUN SHIELD BROAD SPECTRUM SPF 50 MATTE
Brand name suffix SUNSCREEN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/g OCTISALATE 50 mg/g ZINC OXIDE 165 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup 4X49Y0596W Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# 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 SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN 28 g in 1 TUBE LOTION 28 5 62032-140-09 SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN 1 in 1 CARTON LOTION 1 5 62032-140-09 SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN 85 g in 1 TUBE LOTION 85 5 62032-140-34 SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN 479 g in 1 BOTTLE, PUMP LOTION 479 5 62032-140-09 Obagi Nu-Derm System Normal-Dry Skin Transformation Kit 85 g in 1 TUBE LOTION 85 g 165 mg in 1g 4 62032-140-09 Obagi Nu-Derm Fx System Normal-Oily Skin TransformationComplexion Brightening System 85 g in 1 TUBE LOTION 85 g 165 mg in 1g 4 62032-140-09 Obagi Nu-Derm Fx System Normal-Oily Skin TransformationComplexion Brightening System 1 in 1 CARTON LOTION 50 mg in 1g 4 62032-140-09 Obagi Nu-Derm System Normal-Oily Skin Transformation 85 g in 1 TUBE LOTION 85 g 50 mg in 1g 4 62032-140-09 Obagi Nu-Derm System Normal-Dry Skin Transformation Kit 1 in 1 CARTON LOTION 50 mg in 1g 4 62032-140-09 Obagi Nu-Derm System Normal-Oily Skin Transformation 1 in 1 CARTON LOTION 100 mg in 1g 4 62032-140-05 Obagi Nu-Derm System Normal-Oily Skin Transformation Trial 28 g in 1 TUBE LOTION 28 g 100 mg in 1g 3 62032-140-05 Obagi Nu-Derm System Normal-Dry Skin Transformation Trial 28 g in 1 TUBE LOTION 28 g 50 mg in 1g 3 62032-140-09 Obagi Skintrinsiq Brightening Protocol 1 in 1 CARTON LOTION 100 mg in 1g 3 62032-140-09 Obagi Skintrinsiq Brightening Protocol 85 g in 1 TUBE LOTION 85 g 50 mg in 1g 3 62032-140-09 Obagi-C C-Rx System Normal-Dry Skin Intervention 1 in 1 CARTON LOTION 100 mg in 1g 3 62032-140-09 Obagi-C C-Rx System Normal-Dry Skin Intervention 85 g in 1 TUBE LOTION 85 g 50 mg in 1g 3 62032-140-09 Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin 85 g in 1 TUBE LOTION 85 g 100 mg in 1g 3 62032-140-09 Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System 1 in 1 CARTON LOTION 50 mg in 1g 3 62032-140-09 Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin 1 in 1 CARTON LOTION 100 mg in 1g 3 62032-140-09 Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System 85 g in 1 TUBE LOTION 85 g 50 mg in 1g 3 62032-140-05 Obagi Medical Way to Glow Kit 28 g in 1 TUBE LOTION 28 g 50 mg in 1g 2 62032-140-09 Obagi-C C-Rx System Normal-Oily Skin Intervention 85 g in 1 TUBE LOTION 85 g 50 mg in 1g 1 62032-140-09 Obagi-C C-Rx System Normal-Oily Skin Intervention 1 in 1 CARTON LOTION 50 mg in 1g 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62032-140 OBAGI SKINTRINSIQ BRIGHTENING PROTOCOL (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC] 3 Current NDC, Legacy NDC 20250406_2f75ebf7-d6b6-45c6-ad5b-61739d260ff7.zip 62032-140 OBAGI MEDICAL WAY TO GLOW KIT (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC] 2 Current NDC, Legacy NDC 20250406_f6f6e219-4ef6-be3b-e053-6294a90a660d.zip 62032-140 SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) LOTION [OBAGI COSMECEUTICALS LLC] 2 Current NDC, Legacy NDC, 4 package rows 20191102_263ef8e8-e0c4-42e6-bb26-7581a437b35a.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 117 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Total Eye 3-In-1 Renewal Therapy SPF 35 TITANIUM DIOXIDE AND ZINC OXIDE Colorescience 4b116cc4-94d2-4bfc-b7f9-5f486a194c6c 2025-12-16 Warnings Exact identifier application number: M020 Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32 ZINC OXIDE Onekind.25 c11197f4-cee0-04b3-e053-2995a90a1ba8 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Tinted Sunscreen SPF 30 Medium Deep ZINC OXIDE Crunchi, LLC. 69618265-2ebb-4cdc-a28f-e36c07fe5b8f 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Tinted Sunscreen SPF 30 Medium ZINC OXIDE Crunchi, LLC. 23248bc3-1b82-443a-b38a-df7f0efb5d2a 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Tinted Sunscreen SPF 30 Light ZINC OXIDE Crunchi, LLC. cf4039f5-00ee-4227-a3dc-61995c800135 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Body Sunscreen SPF 30 ZINC OXIDE Crunchi, LLC. 227f5a41-8c3c-492d-947f-e2b046208bca 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Tinted Sunscreen SPF 30 Light Medium ZINC OXIDE Crunchi, LLC. 5b3f2766-065b-4817-a5ff-bd1c7882bfc9 2025-12-15 Warnings Exact identifier application number: M020 Crunchi Sunlight Daily Facial Sunscreen SPF 30 ZINC OXIDE Cruchi, LLC. 4f3bcfa0-e43e-4284-afaa-6488ddd749f0 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE The Essential Brazilian Spa LLC 3543a22c-34d5-e572-e063-6394a90ad579 2025-12-15 Exact identifier application number: M020 Stellar Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE The Essential Brazilian Spa LLC 3bb6488c-d216-8742-e063-6394a90a16e2 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE The Essential Brazilian Spa LLC 3bb8ee19-81b2-daed-e063-6394a90a0fb3 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE The Essential Brazilian Spa LLC 3bb6cfd4-fa4a-d1d9-e063-6394a90a8e43 2025-12-15 Warnings Exact identifier application number: M020 Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE The Essential Brazilian Spa LLC 35442ac0-c361-e08f-e063-6294a90a5cb2 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE The Essential Brazilian Spa LLC 3543e85d-9bc7-b8ed-e063-6294a90ae7d3 2025-12-15 Exact identifier application number: M020 Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE The Essential Brazilian Spa LLC 3bc8593d-fc6c-04aa-e063-6394a90a6d56 2025-12-15 Warnings Exact identifier application number: M020 Mineral Sunscreen 20percent Zinc Oxide ZINC OXIDE MANTRA WELLNESS SPA 338855fd-3008-44d9-e063-6294a90a5e07 2025-12-15 Exact identifier application number: M020 Tinted Replenishing Daily Protection ZINC OXIDE MANTRA WELLNESS SPA 33898415-4ee6-a384-e063-6394a90ae8e1 2025-12-15 Exact identifier application number: M020 Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Mantra Wellness Spa 3389b0a3-40f9-b411-e063-6394a90a9959 2025-12-15 Exact identifier application number: M020 Mineral Sunscreen 20percent Zinc Oxide ZINC OXIDE Mantra Wellness Spa 338a11fb-24c6-8a0b-e063-6294a90a761e 2025-12-15 Exact identifier application number: M020 Tinted Replenishing Daily Protection ZINC OXIDE Mantra Wellness Spa 338aa5a2-29e3-fe0e-e063-6294a90a18fd 2025-12-15 Exact identifier application number: M020
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62032-140-05 62032014005 28 g in 1 TUBE (62032-140-05) 28 g 2019-07-15 0000-00-00 No No Current 62032-140-09 62032014009 1 TUBE in 1 CARTON (62032-140-09) / 85 g in 1 TUBE 1 tube 2019-07-15 0000-00-00 No No Current 62032-140-34 62032014034 479 g in 1 BOTTLE, PUMP (62032-140-34) 479 g 2019-07-15 0000-00-00 No No Current