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United States Β· US Β· US:15631-2812_1a236753-b79c-10f8-e063-6294a90ab3f9

LACHESIS M

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerRxhomeo Private Limited d.b.a. Rxhomeo, Inc
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 2

  • ndc11
    1563128120
    10 mL in 1 BOTTLE (15631-2812-0)
  • ndc11
    1563128121
    30 mL in 1 BOTTLE (15631-2812-1)

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": "ORAL",
  "spl_meta": {
    "7243b1d1-b8fb-4eaf-8145-4c3bd6258765": {
      "match": "brand_token",
      "title": "LACHESIS MUTUS 7124 (LACHESIS MUTUS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "15631-2812_1a236753-b79c-10f8-e063-6294a90ab3f9",
  "productndc": "15631-2812",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LACHESIS MUTA VENOM",
  "proprietary_name": "LACHESIS M",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "LACHESIS M",
  "start_marketing_date": "20240523",
  "active_numerator_strength": "8"
}

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LACHESIS M (US) β€” Drug Database