NDC 57293-4401

Fatigue Release

Arnica Montana, Bellis Perennis, Tribasic Calcium Phosphate, Gelsemium Sempervirens Root, Dibasic Potassium Phosphate, Strychnos Nux-vomica Seed, Veratrum Album Root

Fatigue Release is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioenergetics, Inc.. The primary component is Arnica Montana; Bellis Perennis; Tribasic Calcium Phosphate; Gelsemium Sempervirens Root; Dibasic Potassium Phosphate; Strychnos Nux-vomica Seed; Veratrum Album Root.

Product ID57293-4401_68650b80-e426-960f-e053-2991aa0ac274
NDC57293-4401
Product TypeHuman Otc Drug
Proprietary NameFatigue Release
Generic NameArnica Montana, Bellis Perennis, Tribasic Calcium Phosphate, Gelsemium Sempervirens Root, Dibasic Potassium Phosphate, Strychnos Nux-vomica Seed, Veratrum Album Root
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1988-12-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBioEnergetics, Inc.
Substance NameARNICA MONTANA; BELLIS PERENNIS; TRIBASIC CALCIUM PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; DIBASIC POTASSIUM PHOSPHATE; STRYCHNOS NUX-VOMICA SEED; VERATRUM ALBUM ROOT
Active Ingredient Strength6 [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 57293-4401-2

60 mL in 1 BOTTLE, GLASS (57293-4401-2)
Marketing Start Date1988-12-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57293-4401-2 [57293440102]

Fatigue Release LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-12-10

Drug Details

Active Ingredients

IngredientStrength
ARNICA MONTANA6 [hp_X]/60mL

OpenFDA Data

SPL SET ID:aa0e9bd0-36ae-465c-9691-aba912266975
Manufacturer
UNII
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