BOBA HOMO

UNIISPL

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

Identification

ManufacturerDeseret Biologicals, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4374217161
30 mL in 1 BOTTLE, DROPPER (43742-1716-1)

Annotations

UNII (FDA Substance ID)

1948X6KEG3

BABESIA MICROTI

RxCUI 1435869

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1948X6KEG3",
    "rxcui": "1435869",
    "inchikey": null,
    "display_name": "BABESIA MICROTI",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "dae13222-a407-4982-8caf-17397a815806": {
      "match": "brand_token",
      "title": "BOBA HOMO (BABESIA MICROTI, BORRELIA BURGDORFERI NOSODE) LIQUID [DESERET BIOLOGICALS, INC.]",
      "spl_version": "4",
      "published_date": "2024-02-21"
    }
  },
  "productid": "43742-1716_f295efbe-3601-4453-b423-bd493d11ade7",
  "productndc": "43742-1716",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BABESIA MICROTI; BORRELIA BURGDORFERI",
  "proprietary_name": "BOBA HOMO",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Babesia Microti, Borrelia Burgdorferi Nosode",
  "start_marketing_date": "20201007",
  "active_numerator_strength": "15; 15"
}

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