NDC 52731-7031

Fever Complex

Aconitum Napellus, Arnica Montana, Baptisia Tinctoria, Berberis Vulgaris, Cactus Grandiflorus,chelidonium Majus, Echinacea Angustifolia, Ferrum Phosphoricum, Hepar Sulfuris Calcareum, Urtica Urens

Fever Complex is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Nova Homeopathic Therapeutics, Inc.. The primary component is Aconitum Napellus; Arnica Montana; Baptisia Tinctoria Root; Berberis Vulgaris Root Bark; Selenicereus Grandiflorus Stem; Chelidonium Majus; Echinacea Angustifolia; Ferrum Phosphoricum; Calcium Sulfide; Urtica Urens.

Product ID52731-7031_b560a5ff-c533-43ab-9412-a3a2a014f0fd
NDC52731-7031
Product TypeHuman Otc Drug
Proprietary NameFever Complex
Generic NameAconitum Napellus, Arnica Montana, Baptisia Tinctoria, Berberis Vulgaris, Cactus Grandiflorus,chelidonium Majus, Echinacea Angustifolia, Ferrum Phosphoricum, Hepar Sulfuris Calcareum, Urtica Urens
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-06-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNova Homeopathic Therapeutics, Inc.
Substance NameACONITUM NAPELLUS; ARNICA MONTANA; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; SELENICEREUS GRANDIFLORUS STEM; CHELIDONIUM MAJUS; ECHINACEA ANGUSTIFOLIA; FERRUM PHOSPHORICUM; CALCIUM SULFIDE; URTICA URENS
Active Ingredient Strength6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 52731-7031-2

1 BOTTLE in 1 BOX (52731-7031-2) > 50 mL in 1 BOTTLE (52731-7031-1)
Marketing Start Date2011-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52731-7031-1 [52731703101]

Fever Complex LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-06-01

NDC 52731-7031-2 [52731703102]

Fever Complex LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-06-01
Inactivation Date2019-11-13

Drug Details


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