NDC 53346-1373

DR. RECKEWEG R73 Spondarthrin Combination product

Arnica Montana, Radix 4x, Bryonia 4x, Ledum Palustre 4x, Sulphuricum Acidum 6x, Argentum Metallicum 12x, Causticum 12x

DR. RECKEWEG R73 Spondarthrin 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 Arnica Montana Root; Bryonia Dioica Root; Ledum Palustre Twig; Sulfuric Acid; Silver; Causticum.

Product ID53346-1373_bd9bad22-e1d7-439a-83fd-1219b7e6cd87
NDC53346-1373
Product TypeHuman Otc Drug
Proprietary NameDR. RECKEWEG R73 Spondarthrin Combination product
Generic NameArnica Montana, Radix 4x, Bryonia 4x, Ledum Palustre 4x, Sulphuricum Acidum 6x, Argentum Metallicum 12x, Causticum 12x
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1986-06-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NamePHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
Substance NameARNICA MONTANA ROOT; BRYONIA DIOICA ROOT; LEDUM PALUSTRE TWIG; SULFURIC ACID; SILVER; CAUSTICUM
Active Ingredient Strength4 [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 53346-1373-5

50 mL in 1 BOTTLE (53346-1373-5)
Marketing Start Date1986-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53346-1373-5 [53346137305]

DR. RECKEWEG R73 Spondarthrin Combination product LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1986-06-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ARNICA MONTANA ROOT4 [hp_X]/50mL

OpenFDA Data

SPL SET ID:f9aa006c-af8d-45d6-9804-cf407a6c1efb
Manufacturer
UNII
UPC Code
  • 0669330001387

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