58264-0147 : D-139 Sublingual Solution


NDC58264-0147
Labeler: Dna Labs, Inc.
Product Type: Human OTC Drug
Drug Name: D-139
Dosage Form: Sublingual Solution
Rev. Date: 


NDC Package Codes:

  • 58264-0147-1: 29.57 ML IN 1 BOTTLE, GLASS (58264‑0147‑1)

Active Ingredients:

  • Activated Charcoal
  • Anemone Pratensis
  • Arsenic Trioxide
  • Atropa Belladonna
  • Ferrosoferric Phosphate
  • Goldenseal
  • Lycopodium Clavatum Spore
  • Phosphorus
  • Sodium Phosphate
  • Dibasic
  • Heptahydrate
  • Strychnos Nux-vomica Seed

Dosage Strength:

  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 3 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Plant Allergenic Extract [EPC]
  • Plant Proteins [CS]
  • Seed Storage Proteins [CS]

Related Products:

Based on records with the same trade name.
  • 58264-0163 D-139 Sublingual Solution by Dna Labs, Inc.

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.