FDA.reportPublic FDA data

Refy Skin Trio

Manufacturer
Refy
Effective date
2025-11-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:42:31

Label at a glance#

ProductRefy Skin Trio
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Refy Skin Trio

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Refy Skin Trio

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Refy Skin Trio

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Refy Skin Trio

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Refy Skin Trio

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Refy Skin Trio

OTC - PURPOSE SECTION

purposepurpose

Refy Skin Trio

WARNINGS SECTION

Warning LabelWarning Label

Refy Skin Trio

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84047-2090-1Refy Skin Trio36 mL in 1 BOTTLELOTION363
84047-2090-2Refy Skin Trio1 in 1 CARTONLOTION13

Products#

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

DailyMed product names page 1 of 1 · 36 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84047-209084047-2090-1, 84047-2090-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE 1000MCU2324216IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
FERRIC OXIDE RED1K09F3G675IACT
HEXYLENE GLYCOLKEH0A3F75JIACT
LACTIC ACID33X04XA5ATIACT
NIACINAMIDE25X51I8RD4IACT
C13-15 ALKANE114P5I43UJIACT
CHLORELLA VULGARISRYQ4R60M02IACT
ALLANTOIN344S277G0ZIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
CAPRYLYL GLYCOL00YIU5438UIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
GLYCERINPDC6A3C0OXIACT
CAPRYLYL METHICONEQ95M2P1KJLIACT
PRUNUS ARMENIACA (APRICOT) FRUIT269CJD5GZ9IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
PYRUS MALUS (APPLE) FRUITB423VGH5S9IACT
SHEA BUTTER ETHYL ESTERSV2CI786FPGIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
SQUALANEGW89575KF9IACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
WATER059QF0KO0RIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
PROPANEDIOL5965N8W85TIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
SODIUM HYDROXIDE55X04QC32IIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
ZINC OXIDESOI2LOH54ZACTIB
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CHLORIDE451W47IQ8XIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-08-25full-release2026-06-01 01:11:42

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
Refy Skin TrioZINC OXIDERefy3029a690-dbb0-ff15-e063-6394a90abdbe2025-11-06WarningsExact identifier
ndc (package): 84047-2090-2
ndc (package): 84047-2090-1
ndc (product): 84047-2090
ndc11 (package): 84047209001
ndc11 (package): 84047209002
spl id: 42f4dd42-3e3b-36ab-e063-6294a90a91ed
spl set id: 3029a690-dbb0-ff15-e063-6394a90abdbe

Reported adverse events (FAERS/openFDA)#

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