NDC 52731-7025

Burn Complex

Aconitum Napellus 12x, Apis Mellifica 4x, Arnica Montana 3x, Berberis Vulgaris 4x, Calendula Officinalis 3x, Cantharis 4x, Carbo Vegetabilis 12x, Causticum 3x, Echinacea Angustifolia 3x,glonoinum 6x,

Burn 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; Apis Mellifera; Arnica Montana; Berberis Vulgaris Root Bark; Calendula Officinalis Flowering Top; Lytta Vesicatoria; Activated Charcoal; Causticum; Echinacea Angustifolia; Nitroglycerin; Hypericum Perforatum; Urtica Urens.

Product ID52731-7025_5ca4be61-0d88-4635-bf1f-c65587f33162
NDC52731-7025
Product TypeHuman Otc Drug
Proprietary NameBurn Complex
Generic NameAconitum Napellus 12x, Apis Mellifica 4x, Arnica Montana 3x, Berberis Vulgaris 4x, Calendula Officinalis 3x, Cantharis 4x, Carbo Vegetabilis 12x, Causticum 3x, Echinacea Angustifolia 3x,glonoinum 6x,
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-06-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNova Homeopathic Therapeutics, Inc.
Substance NameACONITUM NAPELLUS; APIS MELLIFERA; ARNICA MONTANA; BERBERIS VULGARIS ROOT BARK; CALENDULA OFFICINALIS FLOWERING TOP; LYTTA VESICATORIA; ACTIVATED CHARCOAL; CAUSTICUM; ECHINACEA ANGUSTIFOLIA; NITROGLYCERIN; HYPERICUM PERFORATUM; URTICA URENS
Active Ingredient Strength12 [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; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 52731-7025-2

1 BOTTLE in 1 BOX (52731-7025-2) > 50 mL in 1 BOTTLE (52731-7025-1)
Marketing Start Date2011-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52731-7025-1 [52731702501]

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

NDC 52731-7025-2 [52731702502]

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

Drug Details


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