FDA.reportPublic FDA data

Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin

Product NDC
62032-917
11-digit product format
620320917
Labeler code
62032
Product ID
62032-917_a27a6106-f8cb-47e4-8e71-1f7dceb77d3d
Type
HUMAN OTC DRUG
Nonproprietary name
HOMOSALATE, OCTISALATE, ZINC OXIDE
Dosage form
KIT
Labeler
Obagi Cosmeceuticals LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-12-02
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage62032-91762032-917-01DDiscontinued by firm2026-09-14

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
Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin
Listing expiration
2027-12-31

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
321e58d0-9964-4da9-af6b-66ba81b60cf7Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62032-140-09Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin1 in 1 CARTONLOTION100 mg in 1g3
62032-140-09Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin85 g in 1 TUBELOTION85 g100 mg in 1g3
62032-917-01Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin1 in 1 CARTONKIT13

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
Obagi-C Fx System Normal-Oily Skin Brightening System with ArbutinHOMOSALATE, OCTISALATE, ZINC OXIDEObagi Cosmeceuticals LLC321e58d0-9964-4da9-af6b-66ba81b60cf72026-01-26WarningsExact identifier
ndc (product): 62032-917

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
62032-140-09620320140091 in 1 CARTONHistorical
62032-917-01620320917011 in 1 CARTONHistorical