nu-derm blender skin lightener and blending

Generic: hydroquinone

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

Drug Facts

Product Profile

Brand Name nu-derm blender skin lightener and blending
Generic Name hydroquinone
Labeler obagi cosmeceuticals llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

hydroquinone 40 mg/g

Manufacturer
Obagi Cosmeceuticals LLC

Identifiers & Regulatory

Product NDC 62032-100
Product ID 62032-100_fbe3d3a3-ebf3-425c-9cd5-7b7d26054792
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 1988-01-01

Pharmacologic Class

Established (EPC)
melanin synthesis inhibitor [epc]
Mechanism of Action
melanin synthesis inhibitors [moa]
Physiologic Effect
depigmenting activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62032100
Hyphenated Format 62032-100

Supplemental Identifiers

RxCUI
197795
UPC
0362032100364 0362032116365 0362032101361
UNII
4Y5P7MUD51 XV74C1N1AE 95OOS7VE0Y
NUI
N0000175851 N0000175854 N0000175850

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 blender skin lightener and blending (source: ndc)
Generic Name hydroquinone (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/g
source: ndc
Packaging
  • 28 g in 1 BOTTLE, PLASTIC (62032-100-10)
  • 57 g in 1 BOTTLE, PLASTIC (62032-100-36)
source: ndc

Packages (2)

62032-100-10 28 g in 1 BOTTLE, PLASTIC (62032-100-10) 62032-100-36 57 g in 1 BOTTLE, PLASTIC (62032-100-36)

Ingredients (1)

hydroquinone (40 mg/g)

Linked Drug Pages (1)

NU-DERM BLENDER Skin Lightener and Blending, NU-DERM CLEAR Skin Bleaching and Corrector, NU-DERM SUNFADER Skin Lightener with Sunscreen (SPF 15) PABA FREE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "fbe3d3a3-ebf3-425c-9cd5-7b7d26054792", "openfda": {"nui": ["N0000175851", "N0000175854", "N0000175850"], "upc": ["0362032100364", "0362032116365", "0362032101361"], "unii": ["4Y5P7MUD51", "XV74C1N1AE", "95OOS7VE0Y"], "rxcui": ["197795"], "spl_set_id": ["e5c450af-958e-41e3-9c2f-fda76b3596f5"], "pharm_class_pe": ["Depigmenting Activity [PE]"], "pharm_class_epc": ["Melanin Synthesis Inhibitor [EPC]"], "pharm_class_moa": ["Melanin Synthesis Inhibitors [MoA]"], "manufacturer_name": ["Obagi Cosmeceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28 g in 1 BOTTLE, PLASTIC (62032-100-10)", "package_ndc": "62032-100-10", "marketing_start_date": "19880101"}, {"sample": false, "description": "57 g in 1 BOTTLE, PLASTIC (62032-100-36)", "package_ndc": "62032-100-36", "marketing_start_date": "19880101"}], "brand_name": "NU-DERM BLENDER Skin Lightener and Blending", "product_id": "62032-100_fbe3d3a3-ebf3-425c-9cd5-7b7d26054792", "dosage_form": "CREAM", "pharm_class": ["Depigmenting Activity [PE]", "Melanin Synthesis Inhibitor [EPC]", "Melanin Synthesis Inhibitors [MoA]"], "product_ndc": "62032-100", "generic_name": "HYDROQUINONE", "labeler_name": "Obagi Cosmeceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NU-DERM BLENDER", "brand_name_suffix": "Skin Lightener and Blending", "active_ingredients": [{"name": "HYDROQUINONE", "strength": "40 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19880101", "listing_expiration_date": "20261231"}