nu-derm system normal-dry skin transformation

Generic: hydroquinone, octisalate and zinc oxide

Labeler: obagi cosmeceutical llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name nu-derm system normal-dry skin transformation
Generic Name hydroquinone, octisalate and zinc oxide
Labeler obagi cosmeceutical llc
Dosage Form KIT
Manufacturer
OBAGI COSMECEUTICAL LLC

Identifiers & Regulatory

Product NDC 62032-529
Product ID 62032-529_ed79404d-956a-4f71-b348-3e89930fac3d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2019-12-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62032529
Hyphenated Format 62032-529

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 nu-derm system normal-dry skin transformation (source: ndc)
Generic Name hydroquinone, octisalate and zinc oxide (source: ndc)

Resolved Composition

Strengths
  • 57 g
  • 28 g
  • 10 %
  • 5 %
  • 16.5 %
source: label
Packaging
  • 1 KIT in 1 CARTON (62032-529-06) * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE (62032-141-10) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 198 mL in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

62032-529-06 1 KIT in 1 CARTON (62032-529-06) * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE (62032-141-10) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 198 mL in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

nu-derm system normal-dry skin transformation ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "ed79404d-956a-4f71-b348-3e89930fac3d", "openfda": {"rxcui": ["197795"], "spl_set_id": ["7548658a-5371-4aed-baf8-e5dc54262223"], "manufacturer_name": ["OBAGI COSMECEUTICAL LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (62032-529-06)  *  57 g in 1 BOTTLE, PLASTIC *  57 g in 1 BOTTLE, PLASTIC (62032-100-36)  *  48 g in 1 BOTTLE, PLASTIC *  85 g in 1 TUBE (62032-141-10)  *  57 g in 1 BOTTLE, PLASTIC (62032-101-36)  *  198 mL in 1 BOTTLE, PLASTIC *  198 mL in 1 BOTTLE, PLASTIC", "package_ndc": "62032-529-06", "marketing_start_date": "20191202"}], "brand_name": "nu-derm system normal-dry skin transformation", "product_id": "62032-529_ed79404d-956a-4f71-b348-3e89930fac3d", "dosage_form": "KIT", "product_ndc": "62032-529", "generic_name": "Hydroquinone, Octisalate and Zinc Oxide", "labeler_name": "OBAGI COSMECEUTICAL LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "nu-derm system normal-dry", "brand_name_suffix": "skin transformation", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20191202", "listing_expiration_date": "20261231"}