NDC 44911-0497

Fungustat I

Echinacea (angustifolia), Tabebuia Impetiginosa, Abies Nigra, Lycopodium Clavatum, Nux Vomica, Phosphorus, Pulsatilla (pratensis), Sepia, Skatolum, Candida Albicans

Fungustat I is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energique, Inc.. The primary component is Candida Albicans; Echinacea Angustifolia Whole; Handroanthus Impetiginosus Bark; Lycopodium Clavatum Spore; Phosphorus; Picea Mariana Resin; Pulsatilla Pratensis Whole; Sepia Officinalis Juice; Skatole; Strychnos Nux-vomica Seed.

• Product ID: 44911-0497_00dff638-e674-46a1-9bff-55b422f30e97
• NDC: 44911-0497
• Product Type: Human Otc Drug
• Proprietary Name: Fungustat I
• Generic Name: Echinacea (angustifolia), Tabebuia Impetiginosa, Abies Nigra, Lycopodium Clavatum, Nux Vomica, Phosphorus, Pulsatilla (pratensis), Sepia, Skatolum, Candida Albicans
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2019-05-15
• Marketing End Date: 2024-07-23
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Energique, Inc.
• Substance Name: CANDIDA ALBICANS; ECHINACEA ANGUSTIFOLIA WHOLE; HANDROANTHUS IMPETIGINOSUS BARK; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; PICEA MARIANA RESIN; PULSATILLA PRATENSIS WHOLE; SEPIA OFFICINALIS JUICE; SKATOLE; STRYCHNOS NUX-VOMICA SEED
• Active Ingredient Strength: 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• Pharm Classes: Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
• NDC Exclude Flag: N

Packaging

NDC 44911-0497-1

60 mL in 1 BOTTLE, DROPPER (44911-0497-1)

• Marketing Start Date: 2019-05-15
• Marketing End Date: 2024-07-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44911-0497-1 [44911049701]

Fungustat I LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-05-15

Drug Details

Active Ingredients

Ingredient	Strength
ECHINACEA ANGUSTIFOLIA	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 1ec4b1e4-7e5d-4c8e-975e-25708a121f25
• Manufacturer:
  • Energique, Inc.
• UNII:
  • 8E272251DI
  • C88X29Y479
  • QDL83WN8C2
  • 6GLA1946WX
  • 9W945B5H7R
  • 27YLU75U4W
  • 269XH13919
  • 71AOV0W131
  • 4D7G21HDBC
  • VB06AV5US8

NDC Crossover Matching brand name "Fungustat I" or generic name "Echinacea (angustifolia), Tabebuia Impetiginosa, Abies Nigra, Lycopodium Clavatum, Nux Vomica, Phosphorus, Pulsatilla (pratensis), Sepia, Skatolum, Candida Albicans"

NDC	Brand Name	Generic Name
44911-0108	FUNGUSTAT I	FUNGUSTAT I
44911-0024	Fungustat I	Fungustat I
44911-0119	Fungustat I	Fungustat I
57520-0463	Fungustat I	Fungustat I
57520-0357	Fungustat I	Fungustat I
44911-0497	Fungustat	Echinacea (Angustifolia), Tabebuia Impetiginosa, Abies Nigra, Lycopodium Clavatum, Nux Vomica, Phosphorus, Pulsatilla (Pratensis), Sepia, Skatolum, Candida Albicans
44911-0604	Lymphastat F	Echinacea (Angustifolia), Tabebuia Impetiginosa, Abies Nigra, Lycopodium Clavatum, Nux Vomica, Phosphorus, Pulsatilla (Pratensis), Sepia, Skatolum, Candida Albicans