NDC 50441-0001

PainDefense

Actaea Spicata, Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia, Calcarea Carbonica, Calcarea Fluorica, Causticum, Cimicifuga Racemosa, Formicum Acidum, Hypericum Perforatum, Lemna Minor, Lithium Carbonicum, Magnesia Phosphorica, Phosphorus, Phytolacca Decandra, Pulsatilla, Rhododendron Chrysanthum, Rhus Toxicodendron, Ruta Graveolens, Salicylicum Acidum, Sepia, Zincum Metallicum

PainDefense is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Pharmwest Inc.. The primary component is Actaea Spicata Root; Horse Chestnut; Arnica Montana; Bellis Perennis; Bryonia Alba Root; Oyster Shell Calcium Carbonate, Crude; Calcium Fluoride; Causticum; Black Cohosh; Formic Acid; Hypericum Perforatum; Lemna Minor; Lithium Carbonate; Magnesium Phosphate, Dibasic Trihydrate; Phosphorus; Phytolacca Americana Root; Pulsatilla Vulgaris; Rhododendron Aureum Leaf; Toxicodendron Pubescens Leaf; Ruta Graveolens Flowering Top; Salicylic Acid; Sepia Officinalis Juice; Zinc.

• Product ID: 50441-0001_c8c66c66-0932-4b32-8b8b-80f0972424ca
• NDC: 50441-0001
• Product Type: Human Otc Drug
• Proprietary Name: PainDefense
• Generic Name: Actaea Spicata, Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia, Calcarea Carbonica, Calcarea Fluorica, Causticum, Cimicifuga Racemosa, Formicum Acidum, Hypericum Perforatum, Lemna Minor, Lithium Carbonicum, Magnesia Phosphorica, Phosphorus, Phytolacca Decandra, Pulsatilla, Rhododendron Chrysanthum, Rhus Toxicodendron, Ruta Graveolens, Salicylicum Acidum, Sepia, Zincum Metallicum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-08-06
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: PharmWest Inc.
• Substance Name: ACTAEA SPICATA ROOT; HORSE CHESTNUT; ARNICA MONTANA; BELLIS PERENNIS; BRYONIA ALBA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; CAUSTICUM; BLACK COHOSH; FORMIC ACID; HYPERICUM PERFORATUM; LEMNA MINOR; LITHIUM CARBONATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; RHODODENDRON AUREUM LEAF; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLENS FLOWERING TOP; SALICYLIC ACID; SEPIA OFFICINALIS JUICE; ZINC
• 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; [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 50441-0001-2

59 mL in 1 BOTTLE, SPRAY (50441-0001-2)

• Marketing Start Date: 2013-08-06
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50441-0001-2 [50441000102]

PainDefense LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-08-06
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ACTAEA SPICATA ROOT	10 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: 44f84360-06d0-4e82-9a93-d3e65135c985
• Manufacturer:
  • PharmWest Inc.
• UNII:
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