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United States · US · US:62032-903_cb284faa-845f-4ead-b322-1a7a212a1404
Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Kit
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerObagi Cosmeceuticals LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 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": "62032-903_cb284faa-845f-4ead-b322-1a7a212a1404",
"productndc": "62032-903",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Kit",
"active_ingred_unit": null,
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Homosalate, Octisalate, Zinc Oxide",
"start_marketing_date": "20191202",
"active_numerator_strength": null
}Access this data programmatically
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