NDC 43406-0021

FIBROMYALGIA HP

Aluminum Oxide 30c, Silver Nitrate 30c, Berberis Vulgaris Fruit 30c, Conium Maculatum Flowering Top 30c, Iron 30c, Gelsemium Sempervirens Root 30c, Guaiacum Officinale Resin 30c, Hydrogen 30c, Lachesis Muta Venom 30c, Phosphoric Acid 30c, Toxicodendron Pubescens Leaf 30c

FIBROMYALGIA HP is a Oral Liquid in the Human Prescription Drug category. It is labeled and distributed by Natural Creations, Inc.. The primary component is Aluminum Oxide; Silver Nitrate; Berberis Vulgaris Fruit; Conium Maculatum Flowering Top; Iron; Gelsemium Sempervirens Root; Guaiacum Officinale Resin; Hydrogen; Lachesis Muta Venom; Phosphoric Acid; Toxicodendron Pubescens Leaf.

Product ID43406-0021_b995f789-981d-46b7-93f9-6863a722cdc8
NDC43406-0021
Product TypeHuman Prescription Drug
Proprietary NameFIBROMYALGIA HP
Generic NameAluminum Oxide 30c, Silver Nitrate 30c, Berberis Vulgaris Fruit 30c, Conium Maculatum Flowering Top 30c, Iron 30c, Gelsemium Sempervirens Root 30c, Guaiacum Officinale Resin 30c, Hydrogen 30c, Lachesis Muta Venom 30c, Phosphoric Acid 30c, Toxicodendron Pubescens Leaf 30c
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2007-05-29
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNatural Creations, Inc.
Substance NameALUMINUM OXIDE; SILVER NITRATE; BERBERIS VULGARIS FRUIT; CONIUM MACULATUM FLOWERING TOP; IRON; GELSEMIUM SEMPERVIRENS ROOT; GUAIACUM OFFICINALE RESIN; HYDROGEN; LACHESIS MUTA VENOM; PHOSPHORIC ACID; TOXICODENDRON PUBESCENS LEAF
Active Ingredient Strength30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 43406-0021-1

30 mL in 1 BOTTLE, DROPPER (43406-0021-1)
Marketing Start Date2007-05-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43406-0021-1 [43406002101]

FIBROMYALGIA HP LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-05-29
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
ALUMINUM OXIDE30 [hp_C]/mL

OpenFDA Data

SPL SET ID:9d6654c8-3c7b-4717-af97-6bc53e6adb3d
Manufacturer
UNII
UPC Code
  • 0877730001375

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.