44911-0024 : Fungustat Oral Liquid


NDC: 44911-0024
Labeler: Energique, Inc.
Product Type: Human OTC Drug
Drug Name: Fungustat I
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 44911-0024-1: 30 ML IN 1 BOTTLE, DROPPER (44911‑0024‑1)

Active Ingredients:

  • Echinacea
  • Unspecified
  • Tabebuia Impetiginosa Bark
  • Picea Mariana Resin
  • Lycopodium Clavatum Spore
  • Strychnos Nux-vomica Seed
  • Phosphorus
  • Pulsatilla Vulgaris
  • Sepia Officinalis Juice
  • Skatole
  • Candida Albicans

Dosage Strength:

  • 3 [hp_X]/mL
  • 3 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 15 [hp_X]/mL
  • 30 [hp_X]/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 44911-0108 Fungustat Oral Liquid by Energique, Inc.
  • 44911-0497 Fungustat Oral Liquid by Energique, Inc.
  • 44911-0119 Fungustat Oral Liquid by Energique, Inc
  • 57520-0357 Fungustat Oral Liquid by Apotheca Company
  • 57520-0463 Fungustat Oral Liquid by Apotheca Company

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.