Obagi Nu-Derm Fx System Normal-Dry Skin Transformation

Product NDC
62032-924
11-digit product format
620320924
Labeler code
62032
Product ID
62032-924_02ec7b7b-5758-4141-8603-e9a7ebbe0637
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Zinc Oxide
Dosage form
KIT
Labeler
Obagi Cosmeceuticals LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
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 Fx System Normal-Dry Skin Transformation
Brand name suffix
Complexion Brightening System
Listing expiration
2026-12-31

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
62032-811-09Obagi Nu-Derm Fx System Normal-Dry Skin TransformationComplexion Brightening System85 g in 1 TUBELOTION85 g15.6 g in 100g1
62032-811-09Obagi Nu-Derm Fx System Normal-Dry Skin TransformationComplexion Brightening System1 in 1 CARTONLOTION6.2 g in 100g1
62032-924-01Obagi Nu-Derm Fx System Normal-Dry Skin TransformationComplexion Brightening System1 in 1 BAGKIT11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62032-811-096203208110985 g in 1 TUBE85 gHistorical
62032-924-01620320924011 KIT in 1 BAG (62032-924-01) * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC1 kit2025-06-25NoNoHistorical