NDC 52731-7002

Cold Complex

Aconitum Napellus, Apis Mellifica, Belladonna, Calcarea Carbonica, Echinacea Angustifolia, Euphorbium Officinarum, Kali Bichronicum, Natrum Muriaticum, Nux Vomica, Pulsatilla

Cold 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; Atropa Belladonna; Oyster Shell Calcium Carbonate, Crude; Echinacea Angustifolia; Euphorbia Resinifera Resin; Potassium Dichromate; Sodium Chloride; Strychnos Nux-vomica Seed; Pulsatilla Vulgaris.

Product ID52731-7002_b0a40991-b9be-4194-b3f4-9fba1292e267
NDC52731-7002
Product TypeHuman Otc Drug
Proprietary NameCold Complex
Generic NameAconitum Napellus, Apis Mellifica, Belladonna, Calcarea Carbonica, Echinacea Angustifolia, Euphorbium Officinarum, Kali Bichronicum, Natrum Muriaticum, Nux Vomica, Pulsatilla
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; ATROPA BELLADONNA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ECHINACEA ANGUSTIFOLIA; EUPHORBIA RESINIFERA RESIN; POTASSIUM DICHROMATE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PULSATILLA VULGARIS
Active Ingredient Strength4 [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 52731-7002-2

1 BOTTLE in 1 BOX (52731-7002-2) > 50 mL in 1 BOTTLE (52731-7002-1) (52731-7002-1)
Marketing Start Date2011-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52731-7002-1 [52731700201]

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

NDC 52731-7002-2 [52731700202]

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

Drug Details


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