44911-0204 : Fungustat Oral Liquid


NDC: 44911-0204
Labeler: Energique, Inc.
Product Type: Human OTC Drug
Drug Name: Fungustat Ii
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 44911-0204-1: 60 ML IN 1 BOTTLE, DROPPER (44911‑0204‑1)

Active Ingredients:

  • Candida Albicans
  • Echinacea Angustifolia
  • Fucus Vesiculosus
  • Goldenseal
  • Lycopodium Clavatum Spore
  • Phytolacca Americana Root
  • Pulsatilla Pratensis
  • Sepia Officinalis Juice
  • Sodium Chloride
  • Wood Creosote

Dosage Strength:

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

Related Products:

Based on records with the same trade name.
  • 44911-0192 Fungustat Oral Liquid by Energique, Inc.
  • 44911-0407 Fungustat Oral Liquid by Energique, Inc.
  • 44911-0437 Fungustat Oral Liquid by Energique, Inc.

NDC QR Code

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NDC 44911-0204 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.