NDC 55924-0001

Ultra

Ambrosia Artemisiaefolia, Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Helleborus Niger, Hypothalamus, Ignatia Amara, Lycopodium Clavatum, Magnesia Phosphorica, Manganum Metallicum, Nicotinamidum, Phosphorus, Secale Cornutum, Silicea, Solidago Virgaurea, Thymus Serpyllum, Thyroidinum

Ultra is a Oral Liquid in the Human Prescription Drug category. It is labeled and distributed by Soza Clinic. The primary component is Ambrosia Artemisiifolia; Semecarpus Anacardium Juice; Barium Chloride Dihydrate; Oyster Shell Calcium Carbonate, Crude; Tribasic Calcium Phosphate; Fucus Vesiculosus; Helleborus Niger Root; Bos Taurus Hypothalamus; Strychnos Ignatii Seed; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Manganese; Niacinamide; Phosphorus; Claviceps Purpurea Sclerotium; Silicon Dioxide; Solidago Virgaurea Flowering Top; Thymus Serpyllum; Thyroid, Unspecified.

• Product ID: 55924-0001_785dc00b-da8c-415c-908f-a7ee6b23997c
• NDC: 55924-0001
• Product Type: Human Prescription Drug
• Proprietary Name: Ultra
• Generic Name: Ambrosia Artemisiaefolia, Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Helleborus Niger, Hypothalamus, Ignatia Amara, Lycopodium Clavatum, Magnesia Phosphorica, Manganum Metallicum, Nicotinamidum, Phosphorus, Secale Cornutum, Silicea, Solidago Virgaurea, Thymus Serpyllum, Thyroidinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-05-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Soza Clinic
• Substance Name: AMBROSIA ARTEMISIIFOLIA; SEMECARPUS ANACARDIUM JUICE; BARIUM CHLORIDE DIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; FUCUS VESICULOSUS; HELLEBORUS NIGER ROOT; BOS TAURUS HYPOTHALAMUS; STRYCHNOS IGNATII SEED; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MANGANESE; NIACINAMIDE; PHOSPHORUS; CLAVICEPS PURPUREA SCLEROTIUM; SILICON DIOXIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; THYMUS SERPYLLUM; THYROID, UNSPECIFIED
• Active Ingredient Strength: 10 [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL
• Pharm Classes: Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 55924-0001-1

29.6 mL in 1 BOTTLE, SPRAY (55924-0001-1)

• Marketing Start Date: 2013-05-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55924-0001-1 [55924000101]

Ultra LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-05-03
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
AMBROSIA ARTEMISIIFOLIA	10 [hp_X]/29.6mL

OpenFDA Data

• SPL SET ID: 216b6e1f-e0a8-40db-9d19-6e3f16ae0172
• Manufacturer:
  • Soza Clinic
• UNII:
  • 25X51I8RD4
  • 9W34L2CQ9A
  • S6G2NLH4Y7
  • ETJ7Z6XBU4
  • C88X29Y479
  • 0B4FDL9I6P
  • Y0F0BU8RDU
  • 42Z2K6ZL8P
  • 608DGJ6815
  • EL5GJ3U77E
  • 27YLU75U4W
  • 01G9XEA93N
  • 91D9GV0Z28
  • 2E32821G6I
  • 5405K23S50
  • 535G2ABX9M
  • 1NM3M2487K
  • 86H4S6K51N
  • HF539G9L3Q
• UPC Code:
  • 0633726374997

Pharmacological Class

• Blood Coagulation Factor [EPC]
• Increased Coagulation Factor Activity [PE]
• Calcium [CS]
• Cations
• Divalent [CS]
• Calculi Dissolution Agent [EPC]
• Magnesium Ion Exchange Activity [MoA]
• Osmotic Laxative [EPC]
• Osmotic Activity [MoA]
• Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
• Increased Large Intestinal Motility [PE]
• Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
• Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]

NDC Crossover Matching brand name "Ultra" or generic name "Ambrosia Artemisiaefolia, Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Helleborus Niger, Hypothalamus, Ignatia Amara, Lycopodium Clavatum, Magnesia Phosphorica, Manganum Metallicum, Nicotinamidum, Phosphorus, Secale Cornutum, Silicea, Solidago Virgaurea, Thymus Serpyllum, Thyroidinum"

NDC	Brand Name	Generic Name
30142-562	Ultra	Chloroxylenol 0.3%
55910-589	Ultra	Chloroxylenol 0.3%
55924-0001	Ultra	Ambrosia artemisiaefolia, Anacardium orientale, Baryta muriatica, Calcarea carbonica, Calcarea phosphorica, Fucus Vesiculosus, Helleborus niger, Hypothalamus, Ignatia amara, Lycopodium clavatum, Magnesia phosphorica, Manganum metallicum, Nicotinamidum, Phosphorus, Secale Cornutum, Silicea, Solidago virgaurea, Thymus serpyllum, Thyroidinum
64024-956	Ultra	Chloroxylenol 0.3%