NDC 66579-0028

Back, Neck, Muscle, and Joint Injuries Relief

Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia, Calcarea Carbonica, Calcarea Fluorica, Cimicifuga Racemosa, Cobaltum Metallicum, Gnaphalium Polycephalum, Hypericum Perforatum, Kali Carbonicum, Kali Phosphoricum, Magnesia Phosphorica, Oxalicum Acidum, Phosphorus, Rhus Toxicodendron, Ruta Graveolens, Sepia, Zincum Metallicum

Back, Neck, Muscle, and Joint Injuries Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by New Sun Inc.. The primary component is Horse Chestnut; Arnica Montana; Bellis Perennis; Bryonia Alba Root; Oyster Shell Calcium Carbonate, Crude; Calcium Fluoride; Black Cohosh; Cobalt; Pseudognaphalium Obtusifolium; Hypericum Perforatum; Potassium Carbonate; Potassium Phosphate, Dibasic; Magnesium Phosphate, Dibasic Trihydrate; Oxalic Acid Dihydrate; Phosphorus; Toxicodendron Pubescens Leaf; Ruta Graveolens Flowering Top; Sepia Officinalis Juice; Zinc.

Product ID66579-0028_4662f6d8-2b3a-4f2d-8d1a-4662a3514eb6
NDC66579-0028
Product TypeHuman Otc Drug
Proprietary NameBack, Neck, Muscle, and Joint Injuries Relief
Generic NameAesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia, Calcarea Carbonica, Calcarea Fluorica, Cimicifuga Racemosa, Cobaltum Metallicum, Gnaphalium Polycephalum, Hypericum Perforatum, Kali Carbonicum, Kali Phosphoricum, Magnesia Phosphorica, Oxalicum Acidum, Phosphorus, Rhus Toxicodendron, Ruta Graveolens, Sepia, Zincum Metallicum
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2014-09-08
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNew Sun Inc.
Substance NameHORSE CHESTNUT; ARNICA MONTANA; BELLIS PERENNIS; BRYONIA ALBA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; BLACK COHOSH; COBALT; PSEUDOGNAPHALIUM OBTUSIFOLIUM; HYPERICUM PERFORATUM; POTASSIUM CARBONATE; POTASSIUM PHOSPHATE, DIBASIC; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OXALIC ACID DIHYDRATE; PHOSPHORUS; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLENS FLOWERING TOP; SEPIA OFFICINALIS JUICE; ZINC
Active Ingredient Strength10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 66579-0028-2

59 mL in 1 BOTTLE, SPRAY (66579-0028-2)
Marketing Start Date2014-09-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66579-0028-2 [66579002802]

Back, Neck, Muscle, and Joint Injuries Relief LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-09-08
Inactivation Date2020-01-31

Drug Details


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