NDC 15377-012

Bionica Pain Relieving Gel

Arnica, Belladonna, Bellis, Bryonia, Cuprum Acet, Cuprum Sulph, Calendula, Hypericum, Ledum, Rhus Tox, Ruta, Symphytum, Sulphuricum Ac, Calc Fluor, Calc Phos, Calch Sulph, Ferrum Phos, Kali Sulph, Mag Phos, Nat Mur, Nat Phos, Nat Sulphuricum

Bionica Pain Relieving Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Origin Biomed Inc.. The primary component is Arnica Montana Flower; Atropa Belladonna; Bellis Perennis; Bryonia Alba Root; Cupric Acetate; Cupric Sulfate; Calendula Officinalis Flowering Top; Hypericum Perforatum; Ledum Palustre Twig; Toxicodendron Pubescens Leaf; Ruta Graveolens Flowering Top; Comfrey Root; Sulfuric Acid; Calcium Fluoride; Tribasic Calcium Phosphate; Calcium Sulfate Anhydrous; Ferrosoferric Phosphate; Potassium Chloride; Potassium Phosphate, Dibasic; Potassium Sulfate; Magnesium Phosphate, Dibasic Trihydrate; Sodium Sulfate; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate.

Product ID15377-012_db8c3872-fe84-46af-b155-9952d9154926
NDC15377-012
Product TypeHuman Otc Drug
Proprietary NameBionica Pain Relieving Gel
Generic NameArnica, Belladonna, Bellis, Bryonia, Cuprum Acet, Cuprum Sulph, Calendula, Hypericum, Ledum, Rhus Tox, Ruta, Symphytum, Sulphuricum Ac, Calc Fluor, Calc Phos, Calch Sulph, Ferrum Phos, Kali Sulph, Mag Phos, Nat Mur, Nat Phos, Nat Sulphuricum
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2013-10-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameOrigin BioMed Inc.
Substance NameARNICA MONTANA FLOWER; ATROPA BELLADONNA; BELLIS PERENNIS; BRYONIA ALBA ROOT; CUPRIC ACETATE; CUPRIC SULFATE; CALENDULA OFFICINALIS FLOWERING TOP; HYPERICUM PERFORATUM; LEDUM PALUSTRE TWIG; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLENS FLOWERING TOP; COMFREY ROOT; SULFURIC ACID; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; CALCIUM SULFATE ANHYDROUS; FERROSOFERRIC PHOSPHATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM SULFATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM SULFATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Active Ingredient Strength30 [hp_C]/85g; [hp_C]/85g; [hp_C]/85g; [hp_C]/85g; [hp_X]/85g; [hp_X]/85g; [hp_C]/85g; [hp_C]/85g; [hp_C]/85g; [hp_C]/85g; [hp_C]/85g; [hp_X]/85g; [hp_X]/85g; [hp_C]/85g; [hp_X]/85g; [hp_X]/85g; [hp_C]/85g; [hp_X]/85g; [hp_X]/85g; [hp_X]/85g; [hp_C]/85g; [hp_C]/85g; [hp_X]/85g; [hp_X]/85g
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 15377-012-03

1 TUBE in 1 CARTON (15377-012-03) > 85 g in 1 TUBE
Marketing Start Date2013-10-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15377-012-03 [15377001203]

Bionica Pain Relieving Gel GEL
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-10-03
Inactivation Date2019-11-27

Drug Details


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