Drosera

SPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220180141
30 [hp_X] in 1 TUBE (0220-1801-41)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "ORAL",
  "spl_meta": {
    "5ae94676-2b6e-4888-8691-a8aa9a6c59c9": {
      "match": "brand_token",
      "title": "DROSERA COMBINATION 9221 (DROSERA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "0220-1801_0a0c8b9e-1184-adab-e063-6394a90a94cd",
  "productndc": "0220-1801",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DROSERA ROTUNDIFOLIA",
  "proprietary_name": "Drosera",
  "active_ingred_unit": "[hp_X]/30[hp_X]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "DROSERA ROTUNDIFOLIA",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "30"
}

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