NDC 53346-1343

DR. RECKEWEG R43 Herbamine Combination product

Arsenicum Album 8x, Belladonna 30x, Bryonia 12x, Carbo Vegetabilis 30x, Eriodictyon Californicum 12x, Hypophysis Suis 30x, Kali Phosphoricum 30x, Natrum Muriaticum 30x, Natrum Sulphuricum 200x, Veratrum Album 30x

DR. RECKEWEG R43 Herbamine 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 Arsenic Trioxide; Atropa Belladonna; Bryonia Dioica Root; Activated Charcoal; Eriodictyon Californicum Flowering Top; Sus Scrofa Pituitary Gland; Potassium Phosphate, Dibasic; Sodium Chloride; Sodium Sulfate; Veratrum Album Root.

Product ID53346-1343_db7bf774-b2db-4786-a3f1-cddb90f3fa63
NDC53346-1343
Product TypeHuman Otc Drug
Proprietary NameDR. RECKEWEG R43 Herbamine Combination product
Generic NameArsenicum Album 8x, Belladonna 30x, Bryonia 12x, Carbo Vegetabilis 30x, Eriodictyon Californicum 12x, Hypophysis Suis 30x, Kali Phosphoricum 30x, Natrum Muriaticum 30x, Natrum Sulphuricum 200x, Veratrum Album 30x
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1986-06-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NamePHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
Substance NameARSENIC TRIOXIDE; ATROPA BELLADONNA; BRYONIA DIOICA ROOT; ACTIVATED CHARCOAL; ERIODICTYON CALIFORNICUM FLOWERING TOP; SUS SCROFA PITUITARY GLAND; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; SODIUM SULFATE; VERATRUM ALBUM ROOT
Active Ingredient Strength8 [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 53346-1343-5

50 mL in 1 BOTTLE (53346-1343-5)
Marketing Start Date1986-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53346-1343-5 [53346134305]

DR. RECKEWEG R43 Herbamine Combination product LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1986-06-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ARSENIC TRIOXIDE8 [hp_X]/50mL

OpenFDA Data

SPL SET ID:b6f6670a-0489-41b1-86cb-ca4938fff7bc
Manufacturer
UNII
UPC Code
  • 0669330000892

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