FDA.reportPublic FDA data

No Makeup Concealer (Deep) SPF 20

Manufacturer
N.V. Perricone LLC
Effective date
2023-07-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:55:31

Label at a glance#

ProductNo Makeup Concealer (Deep) SPF 20
Active ingredientZINC OXIDE
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Dosage AdministrationDosage Administration

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

INDICATIONS & USAGE SECTION

Indications UsageIndications Usage

OTC - ACTIVE INGREDIENT SECTION

OTC Active Ingredient SectionOTC Active Ingredient Section

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC keep out of reach of childrenOTC keep out of reach of children

OTC - PURPOSE SECTION

OTC Purpose SectionOTC Purpose Section

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package Label Principle Display Panelpackage Label Principle Display Panel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
124351b2-6dbf-42d0-9ea7-f0e299215f9aProduct name120210115

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
45634-733-932025-01-30C16284748780-12cef2736-686b-d83d-e063-dadaa90ab31fdd916c7e-6fcb-eeea-e053-2995a90a4969

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
45634-733-93No Makeup Concealer (Deep) SPF 2010 g in 1 BOTTLEEMULSION102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
45634-733NO MAKEUP CONCEALER (DEEP) SPF 20 (ZINC OXIDE) EMULSION [N.V. PERRICONE LLC]2Legacy NDC, 1 package rows20230711_dd916c7e-6fcb-eeea-e053-2995a90a4969.zip

Products#

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

DailyMed product names page 1 of 2 · 44 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
45634-73345634-733-93

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 43 matching rows.

Name, UNII, Kind table
NameUNIIKind
MICAV8A1AW0880IACT
ALBIZIA JULIBRISSIN BARK0J9G6W44DVIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
TRICETEARETH-4 PHOSPHATE69534Y66NOIACT
POLYGLYCERYL-6 POLYRICINOLEATEYPM0ZOC2HRIACT
XANTHAN GUMTTV12P4NEEIACT
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE25G622K2RAIACT
DIMETHICONE/PEG-10/15 CROSSPOLYMER21AS8B1BSSIACT
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDEYK3DC63Y5MIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TRIHEPTANOIN2P6O7CFW5KIACT
TRIBEHENIN8OC9U7TQZ0IACT
C13-16 ISOPARAFFINLED42LZG6OIACT
SODIUM CHLORIDE451W47IQ8XIACT
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMERWB5K9Y35Y9IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
DIPROPYLENE GLYCOLE107L85C40IACT
GLYCERINPDC6A3C0OXIACT
ARGAN OIL4V59G5UW9XIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
STANNOUS OXIDEJB2MV9I3LSIACT
SODIUM BENZOATEOJ245FE5EUIACT
SUPEROXIDE DISMUTASE (SACCHAROMYCES CEREVISIAE)W2T4YRA9ADIACT
SODIUM CITRATE1Q73Q2JULRIACT
DARUTOSIDEEG8ODI0780IACT
TOCOPHEROLR0ZB2556P8IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
CYCLOMETHICONE 50THT5PCI0RIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
NYLON-12446U8J075BIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
LEVOMENOL24WE03BX2TIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
OCTYLDODECANOL461N1O614YIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT

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
00232275-64d5-9d37-e063-6294a90a1acbdd916c7e-6fcb-eeea-e053-2995a90a49692023-07-10Exact identifier
spl id: 00232275-64d5-9d37-e063-6294a90a1acb
spl set id: dd916c7e-6fcb-eeea-e053-2995a90a4969

Reported adverse events (FAERS/openFDA)#

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