FDA.reportPublic FDA data

SUNSHINE SKIN TINT BROAD SPECTRUM SPF 30 Sunscreen

Manufacturer
Milk Makeup LLC | COSMAX USA, INC, (COSMAX USA, CORPORATION)
Effective date
2022-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:52:51

Label at a glance#

ProductSUNSHINE SKIN TINT BROAD SPECTRUM SPF 30 Sunscreen
Active ingredientOCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE, OCTISALATE, HOMOSALATE
Label structure1 sections

Label contents#

Full prescribing information#

SUNSHINE SKIN TINT BROAD SPECTRUM SPF 30 pg1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SUNSHINE SKIN TINT BROAD SPECTRUM SPF 30 pg1SUNSHINE SKIN TINT BROAD SPECTRUM SPF 30 pg1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80778-006-032024-01-30C16284748780-10191ceaa-66ce-198a-e063-dbdaa90aec3edad27b2c-9f96-5f72-e053-2a95a90a3483
80778-006-032023-08-09C16284748780-10191ceaa-66ce-198a-e063-dbdaa90aec3edad27b2c-9f96-5f72-e053-2a95a90a3483
80778-006-032023-07-28C16284748780-10191ceaa-66ce-198a-e063-dbdaa90aec3edad27b2c-9f96-5f72-e053-2a95a90a3483

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80778-006-03SUNSHINE SKIN TINT BROAD SPECTRUM SPF 30 Sunscreen16 mL in 1 TUBELOTION162
80778-006-03SUNSHINE SKIN TINT BROAD SPECTRUM SPF 30 Sunscreen1 in 1 CARTONLOTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80778-006SUNSHINE SKIN TINT BROAD SPECTRUM SPF 30 SUNSCREEN LOTION [MILK MAKEUP LLC]2Legacy NDC, 2 package rows20230101_dad27b2c-9f96-5f72-e053-2a95a90a3483.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 46 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80778-00680778-006-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 45 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
OCTOCRYLENE5A68WGF6WMACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB
GRAPE SEED OIL930MLC8XGGIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
HYDROGENATED OLIVE OIL UNSAPONIFIABLESB8MIX97W95IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
SODIUM CHLORIDE451W47IQ8XIACT
OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLESXO45V955LTIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CRAMBE HISPANICA SUBSP. ABYSSINICA SEED OIL0QW9S92J3KIACT
TREMELLA FUCIFORMIS FRUITING BODYGG8N28393GIACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
JOJOBA OIL724GKU717MIACT
GLYCERYL OLEATE4PC054V79PIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
DIISOSTEARYL MALATEQBS8A3XZGQIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
STEARIC ACID4ELV7Z65APIACT
BETAINE3SCV180C9WIACT
PENTYLENE GLYCOL50C1307PZGIACT
OLIVE OIL6UYK2W1W1EIACT
OCTISALATE4X49Y0596WACTIB
TRIBEHENIN8OC9U7TQZ0IACT
XANTHAN GUMTTV12P4NEEIACT
HYDROGENATED JOJOBA OIL, RANDOMIZEDQ47ST02F58IACT
STEARALKONIUM HECTORITEOLX698AH5PIACT
ALUMINUM OXIDELMI26O6933IACT
ACACIA5C5403N26OIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
SQUALANEGW89575KF9IACT
WATER059QF0KO0RIACT
HOMOSALATEV06SV4M95SACTIB
AVOCADO OIL6VNO72PFC1IACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
ISOSTEARIC ACIDX33R8U0062IACT
PHENOXYETHANOLHIE492ZZ3TIACT
FERRIC OXIDE RED1K09F3G675IACT
GLYCERINPDC6A3C0OXIACT

Source Document#

Source XML

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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f124c45b-1113-eba4-e053-2995a90a635cdad27b2c-9f96-5f72-e053-2a95a90a34832022-12-31Exact identifier
spl id: f124c45b-1113-eba4-e053-2995a90a635c
spl set id: dad27b2c-9f96-5f72-e053-2a95a90a3483

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.