NDC 53346-1313

DR. RECKEWEG R13 Prohaemorrhin Combination Product

Aesculus Hippocastanum 2x, Collinsonia Canadensis 4x, Graphites 8x, Hamamelis Virginiana 3x, Kali Carbonicum 6x, Lycopodium Clavatum 5x, Nitricum Acidum 6x, Nux Vomica 4x, Paeonia Officinalis 3x, Sulphur 5x

DR. RECKEWEG R13 Prohaemorrhin Combination Product is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Pharmazeutische Fabrik Dr. Reckeweg & Co. The primary component is Horse Chestnut; Collinsonia Canadensis Root; Graphite; Hamamelis Virginiana Root Bark/stem Bark; Potassium Carbonate; Lycopodium Clavatum Spore; Nitric Acid; Strychnos Nux-vomica Seed; Paeonia Officinalis Root; Sulfur.

Product ID53346-1313_e002f75e-45f8-4b61-8772-0c3d10627e80
NDC53346-1313
Product TypeHuman Otc Drug
Proprietary NameDR. RECKEWEG R13 Prohaemorrhin Combination Product
Generic NameAesculus Hippocastanum 2x, Collinsonia Canadensis 4x, Graphites 8x, Hamamelis Virginiana 3x, Kali Carbonicum 6x, Lycopodium Clavatum 5x, Nitricum Acidum 6x, Nux Vomica 4x, Paeonia Officinalis 3x, Sulphur 5x
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1986-06-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NamePHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
Substance NameHORSE CHESTNUT; COLLINSONIA CANADENSIS ROOT; GRAPHITE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; POTASSIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PAEONIA OFFICINALIS ROOT; SULFUR
Active Ingredient Strength2 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 53346-1313-5

50 mL in 1 BOTTLE (53346-1313-5)
Marketing Start Date1986-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53346-1313-5 [53346131305]

DR. RECKEWEG R13 Prohaemorrhin Combination Product LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1986-06-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
HORSE CHESTNUT2 [hp_X]/50mL

OpenFDA Data

SPL SET ID:b294800f-b158-49aa-86d6-1ba769385076
Manufacturer
UNII
UPC Code
  • 0669330000335

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