NDC 43857-0246

Universaltox

Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubiquinone

Universaltox is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritional, Inc.. The primary component is Alfalfa; Avena Sativa Flowering Top; Fucus Vesiculosus; Hordeum Vulgare Top; Nasturtium Aquaticum; Raphanus Sativus; Triticum Aestivum Whole; Iodine; Ubidecarenone; Sus Scrofa Adrenal Gland; Pork Liver; Manganese Gluconate; Brown Rice; Sus Scrofa Thyroid; Oyster Shell Calcium Carbonate, Crude; Sodium Chloride; Pulsatilla Vulgaris; Toxicodendron Pubescens Leaf; Cortisone Acetate; Paraffin; Ethylene Glycol; Propyl Alcohol; Palmitic Acid; Dimethicone; Sodium Polyacrylate (8000 Mw); Glutaral; Methyl Acrylate; Anhydrous Citric Acid; Tartaric Acid; Anthraquinone; Hydrogen Peroxide; Glycolic Acid; Ammonium Thioglycolate; Sodium Carbonate; Ethanolamine; 2,5-diaminotoluene Sulfate; P-aminophenol.

• Product ID: 43857-0246_58f13b5f-6d26-43e0-849e-12249eb57450
• NDC: 43857-0246
• Product Type: Human Otc Drug
• Proprietary Name: Universaltox
• Generic Name: Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubiquinone
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-01-10
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: BioActive Nutritional, Inc.
• Substance Name: ALFALFA; AVENA SATIVA FLOWERING TOP; FUCUS VESICULOSUS; HORDEUM VULGARE TOP; NASTURTIUM AQUATICUM; RAPHANUS SATIVUS; TRITICUM AESTIVUM WHOLE; IODINE; UBIDECARENONE; SUS SCROFA ADRENAL GLAND; PORK LIVER; MANGANESE GLUCONATE; BROWN RICE; SUS SCROFA THYROID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM CHLORIDE; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; CORTISONE ACETATE; PARAFFIN; ETHYLENE GLYCOL; PROPYL ALCOHOL; PALMITIC ACID; DIMETHICONE; SODIUM POLYACRYLATE (8000 MW); GLUTARAL; METHYL ACRYLATE; ANHYDROUS CITRIC ACID; TARTARIC ACID; ANTHRAQUINONE; HYDROGEN PEROXIDE; GLYCOLIC ACID; AMMONIUM THIOGLYCOLATE; SODIUM CARBONATE; ETHANOLAMINE; 2,5-DIAMINOTOLUENE SULFATE; P-AMINOPHENOL
• 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; [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; [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 43857-0246-1

30 mL in 1 BOTTLE, DROPPER (43857-0246-1)

• Marketing Start Date: 2014-01-10
• Marketing End Date: 2022-06-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43857-0246-1 [43857024601]

Universaltox LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-10
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ALFALFA	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 83f8dec4-2c2b-4d47-a63f-6e4fba12b984
• Manufacturer:
  • BioActive Nutritional, Inc.
• UNII:
  • DJO934BRBD
  • MA9CQJ3F7F
  • 6IO182RP7A
  • R7P8FRP05V
  • I76KB35JEV
  • 5KV86114PT
  • 535G2ABX9M
  • 0WT12SX38S
  • 9679TC07X4
  • 86R5J6D01D
  • 883WKN7W8X
  • EJ27X76M46
  • W4888I119H
  • 2E32821G6I
  • 45P3261C7T
  • 285CYO341L
  • 6EC706HI7F
  • BBX060AN9V
  • 6P9E788VZZ
  • 8PSD05SPE2
  • 3C3Y389JBU
  • 6RV024OAUQ
  • 659G217HPG
  • T3C89M417N
  • 9YY2F980SV
  • FC72KVT52F
  • 030MS0JBDO
  • 96F264O9SV
  • 86507VZR9K
  • WC487PR91H
  • XF417D3PSL
  • 451W47IQ8X
  • 398IYQ16YV
  • 92RU3N3Y1O
  • I9O0E3H2ZE
• Pharm Class PE:
  • Vascular Sclerosing Activity [PE]
• PHarm Class EPC:
  • Sclerosing Agent [EPC]
• NUI Code:
  • N0000020024
  • N0000009905
  • N0000175814

NDC Crossover Matching brand name "Universaltox" or generic name "Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubiquinone"

NDC	Brand Name	Generic Name
43857-0246	Universaltox	Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubiquinone
43857-0534	Universaltox	Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubidecarenonum, Glandula Suprarenalis Suis, Hepar Suis, Manganese Gluconate, Oryza Sativa, Thyroidinum (Suis), Calcarea Carbonica, Natrum Muriaticum, Pulsatilla (Pratensis), Rhus Tox, Cortisone Aceticum