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United States Β· US Β· US:62032-913_f1292c32-db82-4875-b681-b984c56f9cff
Obagi Nu-Derm System Normal-Dry Skin Transformation Trial
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerObagi Cosmeceuticals LLC
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 0
No packs registered.
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"53023b16-8d64-4dfc-bc75-b4f248425c4d": {
"match": "brand_token",
"title": "OBAGI SKINTRINSIQ ANTIOXIDANT PROTOCOL (AVOBENZONE, HOMOSALATE, OCTISALATE. OCTOCRYLENE, AND OXYBENZONE) KIT [OBAGI COSMECEUTICALS LLC]",
"spl_version": "4",
"published_date": "2026-04-30"
}
},
"productid": "62032-913_f1292c32-db82-4875-b681-b984c56f9cff",
"productndc": "62032-913",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Obagi Nu-Derm System Normal-Dry Skin Transformation Trial",
"active_ingred_unit": null,
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE",
"start_marketing_date": "20191202",
"active_numerator_strength": null
}Access this data programmatically
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