FDA.reportPublic FDA data

Obagi Nu-Derm System Normal-Dry Skin Transformation

Product NDC
62032-918
11-digit product format
620320918
Labeler code
62032
Product ID
62032-918_45bc0deb-500d-4616-82e9-c92894c257be
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroquinone, Titanium Dioxide, and Zinc Oxide
Dosage form
KIT
Labeler
Obagi Cosmeceuticals LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2025-06-25
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Obagi Nu-Derm System Normal-Dry Skin Transformation
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
750ea9a6-eedc-49db-8cef-1498ed41ad79Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62032-100-36Obagi Nu-Derm System Normal-Dry Skin Transformation57 g in 1 BOTTLE, PLASTICCREAM57 g40 mg in 1g1
62032-101-36Obagi Nu-Derm System Normal-Dry Skin Transformation57 g in 1 BOTTLE, PLASTICCREAM57 g40 mg in 1g1
62032-811-09Obagi Nu-Derm System Normal-Dry Skin Transformation1 in 1 CARTONLOTION6.2 g in 100g1
62032-811-09Obagi Nu-Derm System Normal-Dry Skin Transformation85 g in 1 TUBELOTION85 g15.6 g in 100g1
62032-918-01Obagi Nu-Derm System Normal-Dry Skin Transformation1 in 1 BAGKIT11

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-Dry Skin TransformationHYDROQUINONE, TITANIUM DIOXIDE, AND ZINC OXIDEObagi Cosmeceuticals LLC750ea9a6-eedc-49db-8cef-1498ed41ad792025-11-04WarningsExact identifier
ndc (product): 62032-918

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197795hydroquinone 4 % Topical CreamPSN750ea9a6-eedc-49db-8cef-1498ed41ad791
197795hydroquinone 40 MG/ML Topical CreamSCD750ea9a6-eedc-49db-8cef-1498ed41ad791
197795hydroquinone 4 % Topical CreamSY750ea9a6-eedc-49db-8cef-1498ed41ad791

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62032-100-366203201003657 g in 1 BOTTLE, PLASTIC57 gHistorical
62032-101-366203201013657 g in 1 BOTTLE, PLASTIC57 gHistorical
62032-811-09620320811091 in 1 CARTONHistorical
62032-918-01620320918011 KIT in 1 BAG (62032-918-01) * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 198 mL in 1 BOTTLE, PLASTIC * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 198 mL in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 57 g in 1 BOTTLE, PLASTIC1 kit2025-06-25NoNoCurrent