FDA.reportPublic FDA data

Dermisa Skin Fade Cream

Manufacturer
RNA PHARMA, LLC
Effective date
2019-12-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:50:02

Label at a glance#

ProductDermisa Skin Fade Cream
Active ingredientHYDROQUINONE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTSACTIVE INGREDIENTSACTIVE INGREDIENTSACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTSINACTIVE INGREDIENTSinactive ingredientsinactive ingredients

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONdosage & administrationdosage & administration

INDICATIONS & USAGE SECTION

INDICATIONS & USAGEINDICATIONS & USAGEindication & usageindication & usage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

OTC - PURPOSE SECTION

purposepurpose

WARNINGS SECTION

warningswarnings

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAYPRINCIPAL DISPLAY

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60717-920-252021-12-22C16284748780-1ba0f9c33-16ce-a910-e053-dadaa90a0b8599ee590c-2263-4cbb-e053-2995a90a5cd0
60717-920-502021-12-22C16284748780-1ba0f9c33-16ce-a910-e053-dadaa90a0b8599ee590c-2263-4cbb-e053-2995a90a5cd0
60717-920-252021-01-29C16284748780-1ba0f9c33-16ce-a910-e053-dadaa90a0b8599ee590c-2263-4cbb-e053-2995a90a5cd0
60717-920-502021-01-29C16284748780-1ba0f9c33-16ce-a910-e053-dadaa90a0b8599ee590c-2263-4cbb-e053-2995a90a5cd0

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-92060717-920-50, 60717-920-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LIMONENE, (+)-GFD7C86Q1WIACT
HYDROXYCITRONELLOLR0B4U2I48WIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM SULFITEVTK01UQK3GIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CETETH-10 PHOSPHATE4E05O5N49GIACT
WATER059QF0KO0RIACT
PROPYLPARABENZ8IX2SC1OHIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
DIHEXADECYL PHOSPHATE2V6E5WN99NIACT
OCTINOXATE4Y5P7MUD51IACT
MINERAL OILT5L8T28FGPIACT
STEARETH-10FD0913P475IACT
STEARETH-2V56DFE46J5IACT
SODIUM METABISULFITE4VON5FNS3CIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
GLYCERINPDC6A3C0OXIACT
PETROLATUM4T6H12BN9UIACT
HYDROQUINONEXV74C1N1AEACTIB

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
d3c3a312-bec2-1c56-e053-2995a90a836299ee590c-2263-4cbb-e053-2995a90a5cd02021-12-22WarningsExact identifier
spl set id: 99ee590c-2263-4cbb-e053-2995a90a5cd0

Reported adverse events (FAERS/openFDA)#

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