D-10

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
5826400101
29.57 mL in 1 BOTTLE, GLASS (58264-0010-1)

Annotations

UNII (FDA Substance ID)

K73E24S6X9

BLACK COHOSH

RxCUI 259511

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "K73E24S6X9",
    "rxcui": "259511",
    "inchikey": null,
    "display_name": "BLACK COHOSH",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "spl_meta": {
    "1e5ba502-eef4-4df0-8330-b70d1872b4bb": {
      "match": "brand_token",
      "title": "D-10 (SEPIA OFFICINALIS WHOLE, SANGUINARIA CANADENSIS ROOT, SULFURIC ACID, BLACK COHOSH, AND LACHESIS MUTA VENOM) SOLUTION [DNA LABS, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-15"
    }
  },
  "productid": "58264-0010_2b9ea65c-9dfb-ad89-e063-6394a90ab44c",
  "productndc": "58264-0010",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BLACK COHOSH; LACHESIS MUTA VENOM; SANGUINARIA CANADENSIS ROOT; SEPIA OFFICINALIS WHOLE; SULFURIC ACID",
  "proprietary_name": "D-10",
  "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": "Sepia officinalis whole, Sanguinaria canadensis root, Sulfuric acid, Black cohosh, and Lachesis muta venom",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "4; 12; 4; 4; 4"
}

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