A-30

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
5826403221
29.57 mL in 1 BOTTLE, GLASS (58264-0322-1)

Annotations

UNII (FDA Substance ID)

6YR2608RSU

TOBACCO LEAF

RxCUI 852062

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6YR2608RSU",
    "rxcui": "852062",
    "inchikey": null,
    "display_name": "TOBACCO LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "spl_meta": {
    "62aab64a-7cb7-46c1-9886-ee0c7ffd0b13": {
      "match": "brand_token",
      "title": "A-30 (TOBACCO LEAF) SOLUTION [DNA LABS, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-13"
    }
  },
  "productid": "58264-0322_2b50cd9c-dbe2-df72-e063-6394a90a53ee",
  "productndc": "58264-0322",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TOBACCO LEAF",
  "proprietary_name": "A-30",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "TOBACCO LEAF",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "30"
}

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