NU-DERM SUNFADER

UNIISPLATC D11AX

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerObagi Cosmeceuticals LLC

CountryUS (United States)

ATC codeD11AX

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6203211636
57 g in 1 BOTTLE, PLASTIC (62032-116-36)

Annotations

UNII (FDA Substance ID)

XV74C1N1AE

HYDROQUINONE

RxCUI 5509

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "XV74C1N1AE",
    "rxcui": "5509",
    "inchikey": "QIGBRXMKCJKVMJ-UHFFFAOYSA-N",
    "display_name": "HYDROQUINONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "4a96c769-4914-4eb8-8530-e4afb80c8c94": {
      "match": "brand_token",
      "title": "NU-DERM SYSTEM NORMAL-OILY SKIN TRANSFORMATION (HYDROQUINONE, HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICAL LLC]",
      "spl_version": "4",
      "published_date": "2025-03-17"
    }
  },
  "productid": "62032-116_fbe3d3a3-ebf3-425c-9cd5-7b7d26054792",
  "productndc": "62032-116",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "HYDROQUINONE; OCTINOXATE; OXYBENZONE",
  "proprietary_name": "NU-DERM SUNFADER",
  "active_ingred_unit": "mg/g; mg/g; mg/g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "HYDROQUINONE, OCTINOXATE, and OXYBENZONE",
  "start_marketing_date": "19840101",
  "active_numerator_strength": "40; 75; 55"
}

Related drugs

Other records sharing ATC code D11AX.

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