Badiaga

UNIISPL

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
0220076141
6 [hp_C] in 1 TUBE (0220-0761-41)

Annotations

UNII (FDA Substance ID)

6SZ0G98BHM

SPONGILLA LACUSTRIS

RxCUI 1330088

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6SZ0G98BHM",
    "rxcui": "1330088",
    "inchikey": null,
    "display_name": "SPONGILLA LACUSTRIS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "1b689f13-59de-9b53-e063-6294a90a296f": {
      "match": "brand_token",
      "title": "BADIAGA COMP. LIQUID [URIEL PHARMACY, INC.]",
      "spl_version": "1",
      "published_date": "2024-07-10"
    }
  },
  "productid": "0220-0761_09ba54aa-8c51-2331-e063-6394a90a8089",
  "productndc": "0220-0761",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SPONGILLA LACUSTRIS",
  "proprietary_name": "Badiaga",
  "active_ingred_unit": "[hp_C]/6[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "SPONGILLA LACUSTRIS",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "6"
}

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