🇺🇸
United States · US · US:62032-100_fbe3d3a3-ebf3-425c-9cd5-7b7d26054792
NU-DERM BLENDER
UNIISPLATC D11AX11
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerObagi Cosmeceuticals LLC
CountryUS (United States)
ATC codeD11AX11
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11620321001028 g in 1 BOTTLE, PLASTIC (62032-100-10)
- ndc11620321003657 g in 1 BOTTLE, PLASTIC (62032-100-36)
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": "62032-100_fbe3d3a3-ebf3-425c-9cd5-7b7d26054792",
"productndc": "62032-100",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "HYDROQUINONE",
"proprietary_name": "NU-DERM BLENDER",
"active_ingred_unit": "mg/g",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "HYDROQUINONE",
"start_marketing_date": "19880101",
"active_numerator_strength": "40"
}Related drugs
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Access this data programmatically
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