obagi nu-derm system normal-oily skin transformation

Generic: hydroquinone, titanium dioxide, zinc oxide

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

Drug Facts

Product Profile

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

Identifiers & Regulatory

Product NDC 62032-919
Product ID 62032-919_41157f8f-7840-42f7-85cd-f16fff7862cc
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2021-06-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62032919
Hyphenated Format 62032-919

Supplemental Identifiers

RxCUI
197795

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 system normal-oily skin transformation (source: ndc)
Generic Name hydroquinone, titanium dioxide, zinc oxide (source: ndc)

Resolved Composition

Strengths
  • 6.2 %
  • 15.6 %
source: label
Packaging
  • 1 KIT in 1 BAG (62032-919-01) * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 48 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-101-36)
source: ndc

Packages (1)

62032-919-01 1 KIT in 1 BAG (62032-919-01) * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 48 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-101-36)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Obagi Nu-Derm System Normal-Oily Skin Transformation ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "41157f8f-7840-42f7-85cd-f16fff7862cc", "openfda": {"rxcui": ["197795"], "spl_set_id": ["ef3ddd1e-9305-42bb-a5f8-559e8e641d83"], "manufacturer_name": ["Obagi Cosmeceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 BAG (62032-919-01)  *  1 TUBE in 1 CARTON (62032-811-09)  / 85 g in 1 TUBE *  198 mL in 1 BOTTLE, PLASTIC *  57 g in 1 BOTTLE, PLASTIC *  198 mL in 1 BOTTLE, PLASTIC *  57 g in 1 BOTTLE, PLASTIC (62032-100-36)  *  48 g in 1 BOTTLE, PLASTIC *  57 g in 1 BOTTLE, PLASTIC (62032-101-36)", "package_ndc": "62032-919-01", "marketing_start_date": "20250625"}], "brand_name": "Obagi Nu-Derm System Normal-Oily Skin Transformation", "product_id": "62032-919_41157f8f-7840-42f7-85cd-f16fff7862cc", "dosage_form": "KIT", "product_ndc": "62032-919", "generic_name": "HYDROQUINONE, TITANIUM DIOXIDE, ZINC OXIDE", "labeler_name": "Obagi Cosmeceuticals LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Obagi Nu-Derm System Normal-Oily Skin Transformation", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210625", "listing_expiration_date": "20261231"}