FDA.reportPublic FDA data

Obagi-C C-Rx System Normal-Oily Skin Intervention

Product NDC
62032-915
Requested package NDC
62032-915-01
11-digit product format
620320915
Labeler code
62032
Product ID
62032-915_d5a6773d-ca09-4b9a-8cbb-4611d29fb7a7
Type
HUMAN OTC DRUG
Nonproprietary name
HYDROQUINONE, 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
2026-12-31
Current FDA listing
Yes

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 C-Rx System Normal-Oily Skin Intervention
Listing expiration
2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
197795Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
e19b824f-4438-48c8-af4c-29be197f9cdcAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62032-105-36Obagi-C C-Rx System Normal-Oily Skin Intervention57 g in 1 BOTTLE, PLASTICCREAM57 g40 mg in 1g1
62032-122-10Obagi-C C-Rx System Normal-Oily Skin Intervention30 mL in 1 BOTTLE, GLASSLIQUID30 mL40 mg in 1mL1
62032-140-09Obagi-C C-Rx System Normal-Oily Skin Intervention85 g in 1 TUBELOTION85 g50 mg in 1g1
62032-140-09Obagi-C C-Rx System Normal-Oily Skin Intervention1 in 1 CARTONLOTION50 mg in 1g1
62032-915-01Obagi-C C-Rx System Normal-Oily Skin Intervention1 in 1 KITKIT11

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 C-Rx System Normal-Oily Skin InterventionHYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDEObagi Cosmeceuticals LLCe19b824f-4438-48c8-af4c-29be197f9cdc2025-10-21WarningsExact identifier
ndc (package): 62032-915-01
ndc (product): 62032-915
ndc11 (package): 62032091501

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197795hydroquinone 4 % Topical CreamPSNe19b824f-4438-48c8-af4c-29be197f9cdc1
197795hydroquinone 40 MG/ML Topical CreamSCDe19b824f-4438-48c8-af4c-29be197f9cdc1
197795hydroquinone 4 % Topical CreamSYe19b824f-4438-48c8-af4c-29be197f9cdc1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62032-915-01620320915011 KIT in 1 KIT (62032-915-01) * 177 mL in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 30 mL in 1 BOTTLE, GLASS (62032-122-10) * 1 TUBE in 1 CARTON (62032-140-09) / 85 g in 1 TUBE * 57 g in 1 BOTTLE, PLASTIC (62032-105-36) 1 kit2021-06-25NoNoCurrent