NDC 59667-0042

Severe Back Pain

Arsenicum 30c, Belladonna 30c, Bryonia 30c, Carbo Animalis 30c, Cinchona 30c, Cina 30c, Colocynthis 30c, Graphites 30c, Ignatia 30c, Lycopodium 30c, Nat Mur 30c, Nitricum Acidum 30c, Rhus Tox

Severe Back Pain is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Home Sweet Homeopathics. The primary component is Arsenic Acid; Atropa Belladonna; Bryonia Alba Root; Carbo Animalis; Cinchona Officinalis Bark; Artemisia Cina Pre-flowering Top; Citrullus Colocynthis Fruit Pulp; Graphite; Strychnos Ignatii Seed; Lycopodium Clavatum Spore; Sodium Chloride; Nitric Acid; Toxicodendron Pubescens Leaf.

Product ID59667-0042_686d297a-422b-4e7e-b669-cdb21a64ffa3
NDC59667-0042
Product TypeHuman Otc Drug
Proprietary NameSevere Back Pain
Generic NameArsenicum 30c, Belladonna 30c, Bryonia 30c, Carbo Animalis 30c, Cinchona 30c, Cina 30c, Colocynthis 30c, Graphites 30c, Ignatia 30c, Lycopodium 30c, Nat Mur 30c, Nitricum Acidum 30c, Rhus Tox
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2013-08-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHome Sweet Homeopathics
Substance NameARSENIC ACID; ATROPA BELLADONNA; BRYONIA ALBA ROOT; CARBO ANIMALIS; CINCHONA OFFICINALIS BARK; ARTEMISIA CINA PRE-FLOWERING TOP; CITRULLUS COLOCYNTHIS FRUIT PULP; GRAPHITE; STRYCHNOS IGNATII SEED; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; NITRIC ACID; TOXICODENDRON PUBESCENS LEAF
Active Ingredient Strength30 [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 59667-0042-2

30 [hp_C] in 1 BOTTLE, SPRAY (59667-0042-2)
Marketing Start Date2013-08-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59667-0042-2 [59667004202]

Severe Back Pain SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-08-02
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
ARSENIC ACID30 [hp_C]/30[hp_C]

OpenFDA Data

SPL SET ID:05fc002c-b306-4e10-9b68-32c3c8a8bf0c
Manufacturer
UNII

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