FDA.reportPublic FDA data

SUN SHIELD BROAD SPECTRUM SPF 50 MATTE

Product NDC
62032-140
Requested package NDC
62032-140-34
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 · 8 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-08-27 00:01 UTC · source 2025-08-26IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

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
IngredientStrength
HOMOSALATE100 mg/g
OCTISALATE50 mg/g
ZINC OXIDE165 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
V06SV4M95SInternal UNII lookup
4X49Y0596WInternal UNII lookup
SOI2LOH54ZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
263ef8e8-e0c4-42e6-bb26-7581a437b35aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
62032-140-052025-10-02SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-092025-10-02SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-342025-10-02SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-052025-01-30SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-092025-01-30SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION
62032-140-342025-01-30SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN LOTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62032-140-05SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN28 g in 1 TUBELOTION285
62032-140-09SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN1 in 1 CARTONLOTION15
62032-140-09SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN85 g in 1 TUBELOTION855
62032-140-34SUN SHIELD BROAD SPECTRUM SPF 50 MATTESUNSCREEN479 g in 1 BOTTLE, PUMPLOTION4795
62032-140-09Obagi Nu-Derm System Normal-Dry Skin Transformation Kit85 g in 1 TUBELOTION85 g165 mg in 1g4
62032-140-09Obagi Nu-Derm Fx System Normal-Oily Skin TransformationComplexion Brightening System85 g in 1 TUBELOTION85 g165 mg in 1g4
62032-140-09Obagi Nu-Derm Fx System Normal-Oily Skin TransformationComplexion Brightening System1 in 1 CARTONLOTION50 mg in 1g4
62032-140-09Obagi Nu-Derm System Normal-Oily Skin Transformation85 g in 1 TUBELOTION85 g50 mg in 1g4
62032-140-09Obagi Nu-Derm System Normal-Dry Skin Transformation Kit1 in 1 CARTONLOTION50 mg in 1g4
62032-140-09Obagi Nu-Derm System Normal-Oily Skin Transformation1 in 1 CARTONLOTION100 mg in 1g4
62032-140-05Obagi Nu-Derm System Normal-Oily Skin Transformation Trial28 g in 1 TUBELOTION28 g100 mg in 1g3
62032-140-05Obagi Nu-Derm System Normal-Dry Skin Transformation Trial28 g in 1 TUBELOTION28 g50 mg in 1g3
62032-140-09Obagi Skintrinsiq Brightening Protocol1 in 1 CARTONLOTION100 mg in 1g3
62032-140-09Obagi Skintrinsiq Brightening Protocol85 g in 1 TUBELOTION85 g50 mg in 1g3
62032-140-09Obagi-C C-Rx System Normal-Dry Skin Intervention1 in 1 CARTONLOTION100 mg in 1g3
62032-140-09Obagi-C C-Rx System Normal-Dry Skin Intervention85 g in 1 TUBELOTION85 g50 mg in 1g3
62032-140-09Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin85 g in 1 TUBELOTION85 g100 mg in 1g3
62032-140-09Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System1 in 1 CARTONLOTION50 mg in 1g3
62032-140-09Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin1 in 1 CARTONLOTION100 mg in 1g3
62032-140-09Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System85 g in 1 TUBELOTION85 g50 mg in 1g3
62032-140-05Obagi Medical Way to Glow Kit28 g in 1 TUBELOTION28 g50 mg in 1g2
62032-140-09Obagi-C C-Rx System Normal-Oily Skin Intervention85 g in 1 TUBELOTION85 g50 mg in 1g1
62032-140-09Obagi-C C-Rx System Normal-Oily Skin Intervention1 in 1 CARTONLOTION50 mg in 1g1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62032-140OBAGI SKINTRINSIQ BRIGHTENING PROTOCOL (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC]3Current NDC, Legacy NDC20250406_2f75ebf7-d6b6-45c6-ad5b-61739d260ff7.zip
62032-140OBAGI MEDICAL WAY TO GLOW KIT (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC]2Current NDC, Legacy NDC20250406_f6f6e219-4ef6-be3b-e053-6294a90a660d.zip
62032-140SUN SHIELD BROAD SPECTRUM SPF 50 MATTE SUNSCREEN (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) LOTION [OBAGI COSMECEUTICALS LLC]2Current NDC, Legacy NDC, 4 package rows20191102_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 1 of 363 · 7,243 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ultra Violette Sheen Screen Broad Spectrum Hydrating Lip Balm DuskSPF50Grace And Fire USA Inc.2735ab0f-5eec-04c5-e063-6394a90aa60e2026-10-01WarningsExact identifier
application number: M020
Ultra Violette Sheen Screen Broad Spectrum Hydrating Lip Balm BejewelledSPF50Grace And Fire USA Inc.274a0544-6c71-4d91-e063-6394a90a22472026-10-01WarningsExact identifier
application number: M020
TRILIPIDERM All-Body Moisture Retention SPF-30AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENETrilipid Research Institute, LLC7f34de0a-eeb3-4b71-9abd-53d03266d9932026-09-10WarningsExact identifier
application number: M020
Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENEKenvue Brands LLC6a43173f-41f9-4207-a0db-53bc8db6f4a42026-09-10WarningsExact identifier
application number: M020
Neutrogena Ultra Sheer Body Mist Sunscreen Broad Spectrum SPF 30AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENEKenvue Brands LLCd69b4992-d7e6-4bd7-b144-0485e35818a62026-09-10WarningsExact identifier
application number: M020
Hydra Finish SPF 15HOMOSALATE, OCTINOXATEGuinot4047e8ec-834a-41e6-a144-5649a7718de42026-09-10WarningsExact identifier
application number: M020
HYDRA BEAUTE SPF 15AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENEGuinot806d1e18-a3fc-43df-a52a-a640902d08872026-09-10WarningsExact identifier
application number: M020
Pur Confort SPF 15AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENEGuinot2fe0656f-f924-48da-91bf-d6f3d98e8fd92026-09-10WarningsExact identifier
application number: M020
Neutrogena Ultra Sheer Body Mist Sunscreen Broad Spectrum SPF 45AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENEKenvue Brands LLC51f3d6ca-3189-4380-9afb-4259ba8782742026-09-10WarningsExact identifier
application number: M020
Sun Logic Creme Solaire Visage et corps SPF 30AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENEGuinotb0a95379-998a-4cda-bae7-63faf3d6f3c82026-09-10WarningsExact identifier
application number: M020
Sun Logic Lait Solaire Corps SPF 20AVOBENZONE, HOMOSALATE, OCTOCRYLENEGuinotd9d2cee0-9189-42d0-b1ab-78b97141b1282026-09-10WarningsExact identifier
application number: M020
SunscreenBROAD SPECTRUM SPF 301226 W AESTHETICS5b0ef395-a7dd-378e-e063-6394a90a5dce2026-09-09WarningsExact identifier
application number: M020
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30W Aesthetics5b0f2c8f-d6fa-5e25-e063-6394a90a084d2026-09-09WarningsExact identifier
application number: M020
Baloom 2% Panthenol Hydro Airy SunscreenAVOBENZONE, HOMOSALATE, OCTISALATE. OCTOCRYLENEARSN KOREA5148b638-f8a4-fa8b-e063-6294a90ac2082026-09-08WarningsExact identifier
application number: M020
Haruharu Wonder - Centella Calm Cloud SPFAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEDFS Company4eee0e75-201c-6d98-e063-6394a90ab7c42026-09-08WarningsExact identifier
application number: M020
Double-Duty Face MoisturizerMOSITURIZING SUNSCREENJack Black, LLC672be406-e3a1-47b4-8ef6-ee2b62baae962026-09-08WarningsExact identifier
application number: M020
Intense Therapy Lip Balm Pineapple MintSUNSCREEN SKIN PROTECTANT LIP BALMJack Black, LLC0862534c-5f48-4f67-a3b8-0876a667556f2026-09-08WarningsExact identifier
application number: M020
Intense Therapy Lip Balm SPF25, Shea Butter and Vitamin ELIP BALM SPF25Jack Black, LLC88e8752d-1fbf-4e28-b79d-7c05ecdce8422026-09-08WarningsExact identifier
application number: M020
Jack Black Intense Lip Therapy SPF25, Natural Mint and Shea ButterLIP BALM SUNSCREENJack Black, LLCe8730127-2d8d-4b80-ab90-d2f136d9e5162026-09-08WarningsExact identifier
application number: M020
Jack Black Intense Therapy Lip Balm SPF25, Grapefruit and GingerLIP BALM SUNSCREENJack Black, LLCd961d22a-2125-41e9-94a3-5b53d12b320f2026-09-08WarningsExact identifier
application number: M020

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197795hydroquinone 4 % Topical CreamPSN16efa2db-8172-4026-a519-08f53d68b3c94
197795hydroquinone 4 % Topical CreamPSNe63327db-fb96-411c-945a-abe801d380454
197795hydroquinone 40 MG/ML Topical CreamSCD16efa2db-8172-4026-a519-08f53d68b3c94
197795hydroquinone 40 MG/ML Topical CreamSCDe63327db-fb96-411c-945a-abe801d380454
197795hydroquinone 4 % Topical CreamSY16efa2db-8172-4026-a519-08f53d68b3c94
197795hydroquinone 4 % Topical CreamSYe63327db-fb96-411c-945a-abe801d380454
197795hydroquinone 4 % Topical CreamPSNca931d1c-4df4-47ce-8d5c-cd8c3e38c02b3
197795hydroquinone 4 % Topical CreamPSNe2c23345-69df-47a1-8e6b-b6225080d3633
197795hydroquinone 4 % Topical CreamPSN219c68dc-1e74-4136-9065-85466008d4453
197795hydroquinone 40 MG/ML Topical CreamSCDca931d1c-4df4-47ce-8d5c-cd8c3e38c02b3
197795hydroquinone 40 MG/ML Topical CreamSCDe2c23345-69df-47a1-8e6b-b6225080d3633
197795hydroquinone 40 MG/ML Topical CreamSCD219c68dc-1e74-4136-9065-85466008d4453
197795hydroquinone 4 % Topical CreamSYca931d1c-4df4-47ce-8d5c-cd8c3e38c02b3
197795hydroquinone 4 % Topical CreamSYe2c23345-69df-47a1-8e6b-b6225080d3633
197795hydroquinone 4 % Topical CreamSY219c68dc-1e74-4136-9065-85466008d4453
197795hydroquinone 4 % Topical CreamPSNe19b824f-4438-48c8-af4c-29be197f9cdc1
197795hydroquinone 40 MG/ML Topical CreamSCDe19b824f-4438-48c8-af4c-29be197f9cdc1
197795hydroquinone 4 % Topical CreamSYe19b824f-4438-48c8-af4c-29be197f9cdc1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62032-140-3462032014034479 g in 1 BOTTLE, PUMP (62032-140-34) 479 g2019-07-150000-00-00NoNoCurrent