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 120 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Daily Skin Protection Sunscreen NT ZINC OXIDE SKINPLUSBYOROYO LLC 35a94d6f-9b1c-1b26-e063-6394a90abe65 2025-12-15 Exact identifier application number: M020 Daily Skin Protection Sunscreen NT ZINC OXIDE SKINPLUSBYOROYO LLC 35a9a6ed-c446-c90c-e063-6294a90aaa74 2025-12-15 Exact identifier application number: M020 Daily Skin Protection Sunscreen Tinted ZINC OXIDE SKINPLUSBYOROYO LLC 35a9ecd7-b416-0aab-e063-6294a90a323d 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer NT TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 3596fe93-836b-4f8e-e063-6294a90a674a 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 359723bb-6152-9566-e063-6294a90a59e0 2025-12-15 Exact identifier application number: M020 Daily Skin Protection Sunscreen Tinted ZINC OXIDE SKINPLUSBYOROYO LLC 35aa194a-9a2e-2b5f-e063-6294a90a9877 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer NT TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 3596cd73-0811-32bc-e063-6394a90ad132 2025-12-15 Exact identifier application number: M020 Proper Protection Plus Primer Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 359782d7-6601-7d96-e063-6394a90af9dc 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 37f1b692-0b80-0536-e063-6294a90ae863 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 387d5194-bc12-68c1-e063-6394a90ab152 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387c23c2-a9f0-f484-e063-6394a90a4104 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387be96f-8cda-ce02-e063-6394a90abea5 2025-12-15 Exact identifier application number: M020 Serum Lightly Tinted ZINC OXIDE PANDA PAMPERING LLC 387c593b-c65b-62b5-e063-6294a90ac4c2 2025-12-15 Exact identifier application number: M020 Serum Lightly Tinted ZINC OXIDE PANDA PAMPERING LLC 387c9167-638c-1e30-e063-6394a90a9374 2025-12-15 Exact identifier application number: M020 REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37ede476-43b6-a7c8-e063-6294a90a3e8f 2025-12-15 Exact identifier application number: M020 REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37efa5e1-e88e-d251-e063-6394a90a9371 2025-12-15 Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd330bf-92e4-3664-e063-6294a90a0475 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd37dd1-fd43-7af4-e063-6394a90ae3a0 2025-12-15 Warnings Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd3dcab-e9fb-0ef5-e063-6394a90acef1 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd40a6a-d52e-ab87-e063-6294a90a966e 2025-12-15 Warnings 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