NDC 68703-105

VaricoGo

Aesculus Hippocastanum, Arnica Montana, Calcarea Fluorica, Carduus Marianus, Carbo Vegetabilis, Collinsonia Canadensis, Echinacea Purpurea, Hamamelis Virginiana, Lachesis Mutus, Pulsatilla, Secale Cornutum

VaricoGo is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies, Llc. The primary component is Horse Chestnut; Arnica Montana; Calcium Fluoride; Activated Charcoal; Silybum Marianum Seed; Collinsonia Canadensis Root; Echinacea Purpurea; Hamamelis Virginiana Root Bark/stem Bark; Lachesis Muta Venom; Pulsatilla Vulgaris; Claviceps Purpurea Sclerotium.

Product ID68703-105_01309f97-f58e-43fa-8fe8-566eea137072
NDC68703-105
Product TypeHuman Otc Drug
Proprietary NameVaricoGo
Generic NameAesculus Hippocastanum, Arnica Montana, Calcarea Fluorica, Carduus Marianus, Carbo Vegetabilis, Collinsonia Canadensis, Echinacea Purpurea, Hamamelis Virginiana, Lachesis Mutus, Pulsatilla, Secale Cornutum
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2013-06-26
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNative Remedies, LLC
Substance NameHORSE CHESTNUT; ARNICA MONTANA; CALCIUM FLUORIDE; ACTIVATED CHARCOAL; SILYBUM MARIANUM SEED; COLLINSONIA CANADENSIS ROOT; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; LACHESIS MUTA VENOM; PULSATILLA VULGARIS; CLAVICEPS PURPUREA SCLEROTIUM
Active Ingredient Strength10 [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 FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68703-105-59

59 mL in 1 BOTTLE, GLASS (68703-105-59)
Marketing Start Date2013-06-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68703-105-59 [68703010559]

VaricoGo SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-06-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
HORSE CHESTNUT10 [hp_X]/59mL

OpenFDA Data

SPL SET ID:00d96b69-41c7-40ba-b76d-1e3237d5c7f0
Manufacturer
UNII
UPC Code
  • 0818837010419

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