NDC 53346-1304

DR. RECKEWEG R4 Enterocolin Combination Product

Baptisia Tinctoria 4x, Chamomilla 4x, Chininum Arsenicosum 6x, Colocynthis 6x, Ferrum Phosphoricum 8x, Mercurius Corrosivus 6x, Oleander 6x, Phosphoricum Acidum 3x, Rhus Toxicodendron 4x, Veratrum Album 6x

DR. RECKEWEG R4 Enterocolin 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 Baptisia Tinctoria Root; Matricaria Recutita; Quinine Arsenite; Citrullus Colocynthis Fruit Pulp; Ferric Phosphate; Mercuric Chloride; Nerium Oleander Leaf; Phosphoric Acid; Toxicodendron Pubescens Leaf; Veratrum Album Root.

Product ID53346-1304_b8455c48-a727-4a2e-8e62-70affad974e3
NDC53346-1304
Product TypeHuman Otc Drug
Proprietary NameDR. RECKEWEG R4 Enterocolin Combination Product
Generic NameBaptisia Tinctoria 4x, Chamomilla 4x, Chininum Arsenicosum 6x, Colocynthis 6x, Ferrum Phosphoricum 8x, Mercurius Corrosivus 6x, Oleander 6x, Phosphoricum Acidum 3x, Rhus Toxicodendron 4x, Veratrum Album 6x
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1986-06-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NamePHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
Substance NameBAPTISIA TINCTORIA ROOT; MATRICARIA RECUTITA; QUININE ARSENITE; CITRULLUS COLOCYNTHIS FRUIT PULP; FERRIC PHOSPHATE; MERCURIC CHLORIDE; NERIUM OLEANDER LEAF; PHOSPHORIC ACID; TOXICODENDRON PUBESCENS LEAF; VERATRUM ALBUM ROOT
Active Ingredient Strength4 [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 53346-1304-5

50 mL in 1 BOTTLE (53346-1304-5)
Marketing Start Date1986-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53346-1304-5 [53346130405]

DR. RECKEWEG R4 Enterocolin Combination Product LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1986-06-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BAPTISIA TINCTORIA ROOT4 [hp_X]/50mL

OpenFDA Data

SPL SET ID:bfc18e81-050b-408d-8544-62387f9be122
Manufacturer
UNII
UPC Code
  • 0669330000090

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