FDA.reportPublic FDA data

YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW

Product NDC
59735-182
11-digit product format
597350182
Labeler code
59735
Product ID
59735-182_4fafb5d1-b38a-dc2e-e063-6394a90a2ce0
Type
HUMAN OTC DRUG
Nonproprietary name
YOUR NAME MINERAL SHEER TINT
Dosage form
CREAM
Route
TOPICAL
Labeler
PML NYC, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2011-02-01
Substance
ZINC OXIDE; TITANIUM DIOXIDE
Active strength
5; 5 g/30mL; g/30mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 5 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct59735-182IInactivated by FDA2026-10-21
excluded packagepackage59735-18259735-182-01IInactivated by FDA2026-10-21
excluded packagepackage59735-18259735-182-04IInactivated by FDA2026-10-21
excluded packagepackage59735-18259735-182-06IInactivated by FDA2026-10-21
excluded packagepackage59735-18259735-182-08IInactivated by FDA2026-10-21

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
YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE5 g/30mL
TITANIUM DIOXIDE5 g/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
SOI2LOH54ZInternal UNII lookup
15FIX9V2JPInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
316c5d69-46f4-7677-e063-6294a90a610fAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
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
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product 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, Related label table
NDCRelated label
59735-182-01YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW
59735-182-04YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW
59735-182-06YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW
59735-182-08YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59735-182-09YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW30 mL in 1 TUBECREAM308
59735-182-10YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW1 in 1 CARTONCREAM18
59735-182-01YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW30 mL in 1 TUBECREAM306
59735-182-01YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW1 in 1 CARTONCREAM16
59735-182-03YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW30 mL in 1 TUBECREAM306
59735-182-04YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW1 in 1 CARTONCREAM16
59735-182-05YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW30 mL in 1 TUBECREAM306
59735-182-06YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW1 in 1 CARTONCREAM16
59735-182-07YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW30 mL in 1 TUBECREAM306
59735-182-08YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW1 in 1 CARTONCREAM16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59735-182YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW (YOUR NAME MINERAL SHEER TINT) CREAM [MANA PRODUCT, INC]7Current NDC, 2 package rows20250331_316c5d69-46f4-7677-e063-6294a90a610f.zip
59735-182YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW (YOUR NAME MINERAL SHEER TINT) CREAM [MANA PRODUCT, INC]6Current NDC, 8 package rows20240808_0e24934c-b25e-51ef-e063-6394a90a2e3f.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 118 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Eclipse Face TintedZINC OXIDEDENISE BELL SKIN CARE396f0151-2d0d-f4da-e063-6394a90a5f7f2025-12-15Exact identifier
application number: M020
Eclipse Body Non TintedZINC OXIDEDENISE BELL SKIN CARE396f56df-d0de-1344-e063-6294a90a46ea2025-12-15Exact identifier
application number: M020
Solar Shield TintedTITANIUM DIOXIDE, ZINC OXIDEDENISE BELL SKIN CARE396eb781-5947-3665-e063-6294a90a38dd2025-12-15Exact identifier
application number: M020
Sun Veil Illuminating Sunscreen SPF30ZINC OXIDEKoco Life LLC46001097-540e-65da-e063-6294a90af2992025-12-15WarningsExact identifier
application number: M020
Mineral Primer tinted SPF40TITANIUM DIOXIDE, ZINC OXIDEOracle Esthetics, LLC3542d8d3-35a3-7d63-e063-6394a90a6fd12025-12-15Exact identifier
application number: M020
Mineral Primer non-tinted SPF40TITANIUM DIOXIDE, ZINC OXIDEOracle Esthetics, LLC354357de-1a85-3bdb-e063-6294a90aa9a22025-12-15Exact identifier
application number: M020
Mineral Primer tinted SPF40TITANIUM DIOXIDE, ZINC OXIDEOracle Esthetics, LLC35433254-1dc8-a8f3-e063-6394a90a29f02025-12-15Exact identifier
application number: M020
Sun Therapy SunscreenZINC OXIDESkin Therapy Studio LLC3544916b-3f63-3a7a-e063-6394a90ae5072025-12-15Exact identifier
application number: M020
Ultra Zinc Mineral Non TintedZINC OXIDESkin Therapy Studio LLC3545d603-3d01-c51d-e063-6394a90a15992025-12-15Exact identifier
application number: M020
Sun Therapy SunscreenZINC OXIDESkin Therapy Studio LLC357efafb-aa1c-0d69-e063-6394a90a51352025-12-15Exact identifier
application number: M020
Ultra Zinc Mineral Non TintedZINC OXIDESkin Therapy Studio LLC35806102-6919-116f-e063-6294a90ad9222025-12-15Exact identifier
application number: M020
Complexion Correction Primer Sunscreen clearTITANIUM DIOXIDE, ZINC OXIDEMCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY357eee3c-1c21-5efb-e063-6294a90a4bb72025-12-15Exact identifier
application number: M020
Complexion Correction Tinted Primer SunscreenTITANIUM DIOXIDE, ZINC OXIDEMCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY357e75ec-473e-df76-e063-6294a90a70c72025-12-15Exact identifier
application number: M020
Complexion Correction Tinted Primer SunscreenTITANIUM DIOXIDE, ZINC OXIDEMCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY357f2f62-904a-2234-e063-6394a90aee722025-12-15Exact identifier
application number: M020
Superscreen Daytime Mineral SunscreenZINC OXIDEMCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY357f915a-bd77-350b-e063-6294a90ad27f2025-12-15Exact identifier
application number: M020
Complexion Correction Primer Sunscreen clearTITANIUM DIOXIDE, ZINC OXIDEMCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY357ff025-84ad-6d77-e063-6394a90aad952025-12-15Exact identifier
application number: M020
Complexion Correction Tinted Primer SunscreenTITANIUM DIOXIDE, ZINC OXIDEMCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY358021a2-235b-825b-e063-6394a90a76f52025-12-15Exact identifier
application number: M020
Superscreen Daytime Mineral SunscreenZINC OXIDEMCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY35805e66-18e6-0e45-e063-6294a90afe582025-12-15Exact identifier
application number: M020
Ultra Zinc Physical DefenseZINC OXIDEATLANTA DERMOTOLOGY VEIN & RESEARCH CENTER35474ac4-8a9d-6a84-e063-6394a90a9bad2025-12-15Exact identifier
application number: M020
Ultra Zinc Physical DefenseZINC OXIDEATLANTA DERMOTOLOGY VEIN & RESEARCH CENTER357e315e-8802-ad73-e063-6394a90a24952025-12-15Exact identifier
application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
59735-182-015973501820130 mL in 1 TUBE30 mlHistorical
59735-182-035973501820330 mL in 1 TUBE30 mlHistorical
59735-182-04597350182041 in 1 CARTONHistorical
59735-182-055973501820530 mL in 1 TUBE30 mlHistorical
59735-182-06597350182061 in 1 CARTONHistorical
59735-182-075973501820730 mL in 1 TUBE30 mlHistorical
59735-182-08597350182081 in 1 CARTONHistorical
59735-182-095973501820930 mL in 1 TUBE30 mlHistorical
59735-182-10597350182101 TUBE in 1 CARTON (59735-182-10) / 30 mL in 1 TUBE (59735-182-09) 1 tube2011-02-01NoNoCurrent