D-39

UNIISPL

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

Identification

ManufacturerDNA Labs, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5826400391
29.57 mL in 1 BOTTLE, GLASS (58264-0039-1)

Annotations

UNII (FDA Substance ID)

VSW71SS07I

LACHESIS MUTA VENOM

RxCUI 1310458

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "VSW71SS07I",
    "rxcui": "1310458",
    "inchikey": null,
    "display_name": "LACHESIS MUTA VENOM",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "spl_meta": {
    "0d997878-b973-45aa-a319-9194fcecc5fc": {
      "match": "brand_token",
      "title": "D-39 (LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, PALLADIUM, SAXIFRAGA GRANULATA WHOLE, AND VESPA CRABRO) SOLUTION [DNA LABS, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-15"
    }
  },
  "productid": "58264-0039_2b9ecbda-7107-d64a-e063-6294a90aac9e",
  "productndc": "58264-0039",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; PALLADIUM; SAXIFRAGA GRANULATA WHOLE; VESPA CRABRO",
  "proprietary_name": "D-39",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, PALLADIUM, SAXIFRAGA GRANULATA WHOLE, and Vespa crabro",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "30; 30; 12; 30; 12"
}

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