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United States · US · US:62032-539_0ad34be9-6f0d-446b-8131-94f8e5f453b9
Obagi Nu-Derm FX System Normal - Dry
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 · 1
- ndc1162032539071 KIT in 1 CARTON (62032-539-07) * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC
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": "62032-539_0ad34be9-6f0d-446b-8131-94f8e5f453b9",
"productndc": "62032-539",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Obagi Nu-Derm FX System Normal - Dry",
"active_ingred_unit": null,
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Homosalate, Octisalate, and Zinc Oxide",
"start_marketing_date": "20191202",
"active_numerator_strength": null
}Access this data programmatically
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