NDC 63479-0203

B03 Sinus Relief

Allium Cepa, Calcarea Iodata, Calcarea Sulphurica, Echinacea Angustifolia, Echinacea Purpurea, Euphorbium Officinarum, Hepar Sulphuris Calcareum, Histaminum Hydrochloricum, Hydrastis Canadensis, Kali Bichromicum, Kali Muriaticum, Kali Sulphuricum, Lac Defloratum, Luffa Operculata, Mercurius Sulphuratus Ruber, Phosphorus, Pulsatilla Vulgaris, Saccharum Lactis, Thuja Occidentalis

B03 Sinus Relief is a Sublingual Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Apex Energetics Inc.. The primary component is Lactose, Unspecified Form; Thuja Occidentalis Leafy Twig; Goldenseal; Potassium Dichromate; Potassium Chloride; Potassium Sulfate; Phosphorus; Skim Milk; Calcium Iodide; Echinacea Angustifolia; Echinacea Purpurea; Euphorbia Resinifera Resin; Calcium Sulfide; Histamine Dihydrochloride; Mercuric Sulfide; Onion; Calcium Sulfate Anhydrous; Luffa Operculata Fruit; Pulsatilla Vulgaris.

Product ID63479-0203_bad83f77-e9af-7118-e053-2a95a90aa737
NDC63479-0203
Product TypeHuman Otc Drug
Proprietary NameB03 Sinus Relief
Generic NameAllium Cepa, Calcarea Iodata, Calcarea Sulphurica, Echinacea Angustifolia, Echinacea Purpurea, Euphorbium Officinarum, Hepar Sulphuris Calcareum, Histaminum Hydrochloricum, Hydrastis Canadensis, Kali Bichromicum, Kali Muriaticum, Kali Sulphuricum, Lac Defloratum, Luffa Operculata, Mercurius Sulphuratus Ruber, Phosphorus, Pulsatilla Vulgaris, Saccharum Lactis, Thuja Occidentalis
Dosage FormSolution/ Drops
Route of AdministrationSUBLINGUAL
Marketing Start Date1995-02-15
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameApex Energetics Inc.
Substance NameLACTOSE, UNSPECIFIED FORM; THUJA OCCIDENTALIS LEAFY TWIG; GOLDENSEAL; POTASSIUM DICHROMATE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; PHOSPHORUS; SKIM MILK; CALCIUM IODIDE; ECHINACEA ANGUSTIFOLIA; ECHINACEA PURPUREA; EUPHORBIA RESINIFERA RESIN; CALCIUM SULFIDE; HISTAMINE DIHYDROCHLORIDE; MERCURIC SULFIDE; ONION; CALCIUM SULFATE ANHYDROUS; LUFFA OPERCULATA FRUIT; PULSATILLA VULGARIS
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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63479-0203-1

30 mL in 1 BOTTLE, GLASS (63479-0203-1)
Marketing Start Date1995-02-15
NDC Exclude FlagN
Sample Package?N

Drug Details


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