A-9

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
5826403011
29.57 mL in 1 BOTTLE, GLASS (58264-0301-1)

Annotations

UNII (FDA Substance ID)

EYO007VX98

HOUSE DUST

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "EYO007VX98",
    "rxcui": null,
    "inchikey": null,
    "display_name": "HOUSE DUST",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "spl_meta": {
    "82c6a284-e728-41ba-83be-169aee864de5": {
      "match": "brand_token",
      "title": "A-9 (HOUSE DUST) SOLUTION [DNA LABS, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-13"
    }
  },
  "productid": "58264-0301_2b507a62-be47-0228-e063-6394a90a3aeb",
  "productndc": "58264-0301",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HOUSE DUST",
  "proprietary_name": "A-9",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "House dust",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "30"
}

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