44911-0706 : Lymphastat F Oral Liquid


NDC44911-0706
Labeler: Energique, Inc
Product Type: Human OTC Drug
Drug Name: Lymphastat F
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 44911-0706-1: 30 ML IN 1 BOTTLE, DROPPER (44911‑0706‑1)

Active Ingredients:

  • Candida Albicans
  • Echinacea Angustifolia Whole
  • Handroanthus Impetiginosus Bark
  • Lycopodium Clavatum Spore
  • Phosphorus
  • Picea Mariana Resin
  • Pulsatilla Vulgaris Whole
  • Sepia Officinalis Juice
  • Skatole
  • Sodium Borate
  • Strychnos Nux-vomica Seed
  • Thuja Occidentalis Leafy Twig

Dosage Strength:

  • 30 [hp_X]/mL
  • 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
  • 15 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [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.
  • 44911-0605 Lymphastat F Oral Liquid by Energique, Inc
  • 44911-0708 Lymphastat F Oral Liquid by Energique, Inc
  • 44911-0604 Lymphastat F Oral Liquid by Energique, 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.