obagi nu-derm fx system normal-dry skin transformation complexion brightening system

Generic: titanium dioxide, zinc oxide

Labeler: obagi cosmeceuticals llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name obagi nu-derm fx system normal-dry skin transformation complexion brightening system
Generic Name titanium dioxide, zinc oxide
Labeler obagi cosmeceuticals llc
Dosage Form KIT
Manufacturer
Obagi Cosmeceuticals LLC

Identifiers & Regulatory

Product NDC 62032-924
Product ID 62032-924_02ec7b7b-5758-4141-8603-e9a7ebbe0637
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2025-06-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62032924
Hyphenated Format 62032-924

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name obagi nu-derm fx system normal-dry skin transformation complexion brightening system (source: ndc)
Generic Name titanium dioxide, zinc oxide (source: ndc)
Application Number M020 (source: ndc)

Resolved Composition

Strengths
  • 6.2 %
  • 15.6 %
source: label
Packaging
  • 1 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, PLASTIC
source: ndc

Packages (1)

62032-924-01 1 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, PLASTIC

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "02ec7b7b-5758-4141-8603-e9a7ebbe0637", "openfda": {"spl_set_id": ["4cbf1dc6-78b3-4e51-a53f-2018ac88136a"], "manufacturer_name": ["Obagi Cosmeceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 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, PLASTIC", "package_ndc": "62032-924-01", "marketing_start_date": "20250625"}], "brand_name": "Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System", "product_id": "62032-924_02ec7b7b-5758-4141-8603-e9a7ebbe0637", "dosage_form": "KIT", "product_ndc": "62032-924", "generic_name": "Titanium Dioxide, Zinc Oxide", "labeler_name": "Obagi Cosmeceuticals LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Obagi Nu-Derm Fx System Normal-Dry Skin Transformation", "brand_name_suffix": "Complexion Brightening System", "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250625", "listing_expiration_date": "20261231"}