NDC 57520-0099

FNG II

Echinacea Angustifolia, Hydrastis Canadensis, Lomatium, Nasturtium Aquaticum, Tabebuia Impetiginosa, Iodium, Adrenalinum, Argentum Metallicum, Thymus, Thyroidinum, Phosphoricum Acidum, Candida Albicans, Lycopodium Clavatum, Pulsatilla, Sepia

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

• Product ID: 57520-0099_3715c74f-6dab-456a-bd34-efdd7c629615
• NDC: 57520-0099
• Product Type: Human Otc Drug
• Proprietary Name: FNG II
• Generic Name: Echinacea Angustifolia, Hydrastis Canadensis, Lomatium, Nasturtium Aquaticum, Tabebuia Impetiginosa, Iodium, Adrenalinum, Argentum Metallicum, Thymus, Thyroidinum, Phosphoricum Acidum, Candida Albicans, Lycopodium Clavatum, Pulsatilla, Sepia
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2010-02-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Apotheca Company
• Substance Name: ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; LOMATIUM DISSECTUM ROOT; TABEBUIA IMPETIGINOSA BARK; IODINE; EPINEPHRINE; SILVER; SUS SCROFA THYMUS; THYROID, UNSPECIFIED; PHOSPHORIC ACID; CANDIDA ALBICANS; LYCOPODIUM CLAVATUM SPORE; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; RORIPPA NASTURTIUM-AQUATICUM
• Active Ingredient Strength: 3 [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 57520-0099-1

30 mL in 1 BOTTLE, DROPPER (57520-0099-1)

• Marketing Start Date: 2010-02-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 57520-0099-1 [57520009901]

FNG II LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-02-17
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ECHINACEA ANGUSTIFOLIA	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 562cc0df-a340-4573-88b1-0d4119ec9766
• Manufacturer:
  • Apotheca Company
• UNII:
  • YH89GMV676
  • 7B69B0BD62
  • C88X29Y479
  • ZW3Z11D0JV
  • 6GLA1946WX
  • 3M4G523W1G
  • E4GA8884NN
  • YKH834O4BH
  • 4D7G21HDBC
  • I76KB35JEV
  • 9679TC07X4
  • 5329928G5N
  • QDL83WN8C2
  • 0B4FDL9I6P
  • VB06AV5US8

NDC Crossover Matching brand name "FNG II" or generic name "Echinacea Angustifolia, Hydrastis Canadensis, Lomatium, Nasturtium Aquaticum, Tabebuia Impetiginosa, Iodium, Adrenalinum, Argentum Metallicum, Thymus, Thyroidinum, Phosphoricum Acidum, Candida Albicans, Lycopodium Clavatum, Pulsatilla, Sepia"

NDC	Brand Name	Generic Name
43857-0424	FNG II	FNG II
43857-0317	FNG II	FNG II
57520-0099	FNG	Echinacea angustifolia, Hydrastis canadensis, Lomatium, Nasturtium aquaticum, Tabebuia impetiginosa, Iodium, Adrenalinum, Argentum metallicum, Thymus, Thyroidinum, Phosphoricum acidum, Candida albicans, Lycopodium clavatum, Pulsatilla, Sepia