NDC 57955-2322

Prejudiced

Ferrum Metallicum, Gratiola Officinalis, Hamamelis Virginiana, Helianthus Annuus, Hottonia Palustris, Flos, Lachesis Mutus, Lilium Tigrinum, Lycopodium Clavatum, Moschus, Palladium Metallicum, Platinum Metallicum, Rhus Toxicodendron, Staphysagria, Sulphur, Veratrum Album, Viola Odorata

Prejudiced is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by King Bio Inc.. The primary component is Iron; Gratiola Officinalis; Hamamelis Virginiana Root Bark/stem Bark; Helianthus Annuus Flowering Top; Hottonia Palustris Flower; Lachesis Muta Venom; Lilium Lancifolium Whole Flowering; Lycopodium Clavatum Spore; Moschus Moschiferus Musk Sac Resin; Palladium; Platinum; Toxicodendron Pubescens Leaf; Delphinium Staphisagria Seed; Sulfur; Veratrum Album Root; Viola Odorata.

• Product ID: 57955-2322_2c12444d-b982-4387-b8c0-9c27fade5edf
• NDC: 57955-2322
• Product Type: Human Otc Drug
• Proprietary Name: Prejudiced
• Generic Name: Ferrum Metallicum, Gratiola Officinalis, Hamamelis Virginiana, Helianthus Annuus, Hottonia Palustris, Flos, Lachesis Mutus, Lilium Tigrinum, Lycopodium Clavatum, Moschus, Palladium Metallicum, Platinum Metallicum, Rhus Toxicodendron, Staphysagria, Sulphur, Veratrum Album, Viola Odorata
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-12-12
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: King Bio Inc.
• Substance Name: IRON; GRATIOLA OFFICINALIS; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HELIANTHUS ANNUUS FLOWERING TOP; HOTTONIA PALUSTRIS FLOWER; LACHESIS MUTA VENOM; LILIUM LANCIFOLIUM WHOLE FLOWERING; LYCOPODIUM CLAVATUM SPORE; MOSCHUS MOSCHIFERUS MUSK SAC RESIN; PALLADIUM; PLATINUM; TOXICODENDRON PUBESCENS LEAF; DELPHINIUM STAPHISAGRIA SEED; SULFUR; VERATRUM ALBUM ROOT; VIOLA ODORATA
• Active Ingredient Strength: 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 57955-2322-2

59 mL in 1 BOTTLE, SPRAY (57955-2322-2)

• Marketing Start Date: 2013-12-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 57955-2322-2 [57955232202]

Prejudiced LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-12-12
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
IRON	10 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: 100aa4a7-48c2-40cf-b473-106a3cff0ead
• Manufacturer:
  • King Bio Inc.
• UNII:
  • 70FD1KFU70
  • Q954GT7P3G
  • C88X29Y479
  • 6IO182RP7A
  • BDD9991A36
  • 5TWQ1V240M
  • E1UOL152H7
  • 00543AP1JV
  • QNS6W5US1Z
  • BKJ0J3D1BP
  • VSW71SS07I
  • 8KFK4W7KP7
  • AET12U8B74
  • X67Z2963PI
  • T7S323PKJS
  • 49DFR088MY