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 101 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join COCO AND EVE SUNNY HONEY PROTECT TAN BOOSTING ANTI-AGING SPF 45 SUNSCREEN OIL Soleil Collective LLC 471c0eed-f7ca-3c3b-e063-6294a90ad2c6 2025-12-29 Warnings Exact identifier application number: M020 EIGHT HOUR NOURISHING LIP SPF 20 OCTINOXATE, AVOBENZONE REVLON b3c16e60-752d-6eba-e053-2995a90a2b20 2025-12-29 Warnings Exact identifier application number: M020 CERAMIDE PREMIERE BROAD SPECTRUM SPF 30 OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, AVOBENZONE REVLON b3358bfd-7fe5-33e2-e053-2a95a90ac2ea 2025-12-29 Warnings Exact identifier application number: M020 Prevage anti aging SPF 30 OCTISALATE, OCTINOXATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE, Revlon b2bff796-1579-2686-e053-2995a90ad6c7 2025-12-29 Warnings Exact identifier application number: M020 FLAWLESS FUTURE SPF 30 OCTINOXATE, OCTISALATE, OXYBENZONE, AVAOBENZONE REVLON b553aec1-5002-3a3f-e053-2995a90a22e5 2025-12-29 Warnings Exact identifier application number: M020 Prevage Anti-aging eye cream SPF 15 OCTINOXATE, OXYBENZONE Revlon b2a92d72-e634-7379-e053-2995a90a2bca 2025-12-29 Warnings Exact identifier application number: M020 Prevage Anti-aging Moisture Cream OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, AVOBENZONE Revlon Consumer Products Corp b247adbe-dfe8-df0a-e053-2995a90a34d9 2025-12-29 Warnings Exact identifier application number: M020 Sheer Protection SPF 30 ZINC OXIDE Skin Script, LLC 0450dcc9-3f8f-e2c2-e063-6294a90af60b 2025-12-29 Warnings Exact identifier application number: M020 RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20 OCTINOXATE AND TITANIUM DIOXIDE ESTEE LAUDER INC 897b8edb-f089-4a49-baca-e05806b0a068 2025-12-29 Warnings Exact identifier application number: M020 Mine Line Coconut Sunscreen SPF 50 ZINC OXIDE Spa de Soleil 4642b1cc-43b1-6997-e063-6394a90ac764 2025-12-29 Warnings Exact identifier application number: M020 SnugZ SPF 30 Broad Spectrum Sunscreen SPF 30 BROAD SPECTRUM SUNSCREEN SnugZ/USA, LLC 69ac1218-76e6-04ff-e053-2a91aa0a4080 2025-12-29 Warnings Exact identifier application number: M020 SnugZ SPF 50 Sunscreen Spry SPF 50 SUNSCREEN SPRAY SnugZ USA 9390ea21-9f9f-14e2-e053-2a95a90ac577 2025-12-29 Warnings Exact identifier application number: M020 SnugZ SPF 15 Flavored Beeswax Lip Balm SPF 15 FLAVORED BEESWAX LIP BALM SnugZ/USA, LLC 69bdfaaf-d49e-bf31-e053-2a91aa0affd3 2025-12-29 Warnings Exact identifier application number: M020 SnugZ SPF 50 Broad Spectrum Sunscreen SPF 50 BROAD SPECTRUM SUNSCREEN SnugZ/USA, LLC b7a3eed5-c8ca-ffda-e053-2a95a90a73bb 2025-12-29 Warnings Exact identifier application number: M020 SnugZ SPF 15 Beeswax Lip Balm SPF 15 BEESWAX LIP BALM SnugZ/USA, LLC 68816d3a-dbe9-7ce3-e053-2a91aa0a395e 2025-12-29 Warnings Exact identifier application number: M020 SnugZ SPF 30 Soy Lip Balm SPF 30 SOY LIP BALM SnugZ/USA, LLC 687ff49d-2d0e-2534-e053-2991aa0a2864 2025-12-29 Warnings Exact identifier application number: M020 SnugZ SPF 50 Sunscreen Stick SPF 50 SUNSTICK SnugZ/USA, LLC 6e1179cf-5bfb-1156-e053-2991aa0a5b46 2025-12-29 Warnings Exact identifier application number: M020 OUHOE Face Body Sunscreen TITANIUM DIOXIDE Shantou Ouhoe Technology Co., Ltd. 46d36f60-2a5d-816e-e063-6294a90a2ddc 2025-12-26 Warnings Exact identifier application number: M020 OUHOE Bean Sunscreen TITANIUM DIOXIDE Shantou Ouhoe Technology Co., Ltd. 46d3b11f-93d9-0e38-e063-6294a90a41c3 2025-12-26 Warnings Exact identifier application number: M020 Cream ZINC OXIDE MONAT GLOBAL CORP e922d89c-4232-77d8-e053-2995a90a85e5 2025-12-26 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