Obagi Nu-Derm System Normal-Oily Skin Transformation Trial

Product NDC
62032-914
11-digit product format
620320914
Labeler code
62032
Product ID
62032-914_bc389b46-a94e-4cc3-baec-73044c6a387f
Type
HUMAN PRESCRIPTION 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 Nu-Derm System Normal-Oily Skin Transformation Trial
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
219c68dc-1e74-4136-9065-85466008d445Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62032-101-36Obagi Nu-Derm System Normal-Oily Skin Transformation Trial57 g in 1 BOTTLE, PLASTICCREAM57 g40 mg in 1g3
62032-140-05Obagi Nu-Derm System Normal-Oily Skin Transformation Trial28 g in 1 TUBELOTION28 g100 mg in 1g3
62032-914-01Obagi Nu-Derm System Normal-Oily Skin Transformation Trial1 in 1 KITKIT13

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 Nu-Derm System Normal-Oily Skin Transformation TrialHYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDEObagi Cosmeceuticals LLC219c68dc-1e74-4136-9065-85466008d4452025-10-23WarningsExact identifier
ndc (product): 62032-914

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197795hydroquinone 4 % Topical CreamPSN219c68dc-1e74-4136-9065-85466008d4453
197795hydroquinone 40 MG/ML Topical CreamSCD219c68dc-1e74-4136-9065-85466008d4453
197795hydroquinone 4 % Topical CreamSY219c68dc-1e74-4136-9065-85466008d4453

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62032-101-366203201013657 g in 1 BOTTLE, PLASTIC57 gHistorical
62032-140-056203201400528 g in 1 TUBE28 gHistorical
62032-914-01620320914011 KIT in 1 KIT (62032-914-01) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 28 g in 1 BOTTLE, PLASTIC * 28 g in 1 BOTTLE, PLASTIC * 28 g in 1 TUBE (62032-140-05) * 59 mL in 1 BOTTLE, PLASTIC * 59 mL in 1 BOTTLE, PLASTIC1 kit2021-06-25NoNoCurrent