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United States · US · US:62032-922_379fa44a-bdd2-4048-8b45-1fec370a3788
Obagi-C C-Rx System Normal-Dry Skin Intervention
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
- ndc1162032922011 KIT in 1 BAG (62032-922-01) * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 177 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-105-36) * 1 BOTTLE, GLASS in 1 CARTON (62032-106-10) / 30 mL in 1 BOTTLE, GLASS
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"321e58d0-9964-4da9-af6b-66ba81b60cf7": {
"match": "brand_token",
"title": "OBAGI-C FX SYSTEM NORMAL-OILY SKIN BRIGHTENING SYSTEM WITH ARBUTIN (HOMOSALATE, OCTISALATE, ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC]",
"spl_version": "3",
"published_date": "2026-01-28"
}
},
"productid": "62032-922_379fa44a-bdd2-4048-8b45-1fec370a3788",
"productndc": "62032-922",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Obagi-C C-Rx System Normal-Dry Skin Intervention",
"active_ingred_unit": null,
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "HYDROQUINONE, TITANIUM DIOXIDE, ZINC OXIDE",
"start_marketing_date": "20191202",
"active_numerator_strength": null
}Access this data programmatically
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