NDC 43857-0317

FNG II

Echinacea (angustifolia), Hydrastis Canadensis, Lomatium Dissectum, Nasturtium Aquaticum, Tabebuia Impetiginosa, Iodium, Adrenalinum, Argentum Metallicum, Thymus (suis), Throidinum (suis), Phosphoricum Acidum, Candida Albicans, Lycopodium Clavatum, Pulsatilla (vulgaris), Sepia

FNG II is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritional, Inc.. The primary component is Echinacea Angustifolia; Goldenseal; Lomatium Dissectum Root; Nasturtium Officinale; Tabebuia Impetiginosa Bark; Iodine; Epinephrine; Silver; Sus Scrofa Thymus; Sus Scrofa Thyroid; Phosphoric Acid; Candida Albicans; Lycopodium Clavatum Spore; Pulsatilla Vulgaris; Sepia Officinalis Juice.

• Product ID: 43857-0317_8f38abe9-28a3-49bc-b935-d05fdff9e39c
• NDC: 43857-0317
• Product Type: Human Otc Drug
• Proprietary Name: FNG II
• Generic Name: Echinacea (angustifolia), Hydrastis Canadensis, Lomatium Dissectum, Nasturtium Aquaticum, Tabebuia Impetiginosa, Iodium, Adrenalinum, Argentum Metallicum, Thymus (suis), Throidinum (suis), Phosphoricum Acidum, Candida Albicans, Lycopodium Clavatum, Pulsatilla (vulgaris), Sepia
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-07-15
• Marketing End Date: 2021-01-21
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: BioActive Nutritional, Inc.
• Substance Name: ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; LOMATIUM DISSECTUM ROOT; NASTURTIUM OFFICINALE; TABEBUIA IMPETIGINOSA BARK; IODINE; EPINEPHRINE; SILVER; SUS SCROFA THYMUS; SUS SCROFA THYROID; PHOSPHORIC ACID; CANDIDA ALBICANS; LYCOPODIUM CLAVATUM SPORE; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE
• Active Ingredient Strength: 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; 1/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; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43857-0317-1

30 mL in 1 BOTTLE, DROPPER (43857-0317-1)

• Marketing Start Date: 2014-07-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43857-0317-1 [43857031701]

FNG II LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-07-15
• Marketing End Date: 2021-01-21

Drug Details

Active Ingredients

Ingredient	Strength
ECHINACEA ANGUSTIFOLIA	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: e215f138-e491-47a1-8e8a-005b29bae3b5
• Manufacturer:
  • BioActive Nutritional, Inc.
• UNII:
  • 6RV024OAUQ
  • YH89GMV676
  • 7B69B0BD62
  • C88X29Y479
  • ZW3Z11D0JV
  • 6GLA1946WX
  • 3M4G523W1G
  • YKH834O4BH
  • 4D7G21HDBC
  • I76KB35JEV
  • 9679TC07X4
  • 5329928G5N
  • QDL83WN8C2
  • E4GA8884NN
  • VB06AV5US8

NDC Crossover Matching brand name "FNG II" or generic name "Echinacea (angustifolia), Hydrastis Canadensis, Lomatium Dissectum, Nasturtium Aquaticum, Tabebuia Impetiginosa, Iodium, Adrenalinum, Argentum Metallicum, Thymus (suis), Throidinum (suis), Phosphoricum Acidum, Candida Albicans, Lycopodium Clavatum, Pulsatilla (vulgaris), Sepia"

NDC	Brand Name	Generic Name
43857-0424	FNG II	FNG II
57520-0099	FNG II	FNG II
43857-0317	FNG	Echinacea (Angustifolia), Hydrastis Canadensis, Lomatium Dissectum, Nasturtium Aquaticum, Tabebuia Impetiginosa, Iodium, Adrenalinum, Argentum Metallicum, Thymus (Suis), Throidinum (Suis), Phosphoricum Acidum, Candida Albicans, Lycopodium Clavatum, Pulsatilla (Vulgaris), Sepia