NDC 50845-0184

Unique Pain Reduction Arthritis

Aconitum Napellus, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Colchicum Autumnale, Eupatorium Perfoliatum, Guaiacum, Hypericum Perforatum, Ledum Palustre, Mercurius Corrosivus, Rhus Tox, Thuja Occidentalis

Unique Pain Reduction Arthritis is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Liddell Laboratories, Inc.. The primary component is Aconitum Napellus; Apis Mellifera; Benzoic Acid; Sus Scrofa Cartilage; Colchicum Autumnale Bulb; Eupatorium Perfoliatum Flowering Top; Guaiacum Officinale Resin; Hypericum Perforatum; Ledum Palustre Twig; Mercuric Chloride; Toxicodendron Pubescens Leaf; Thuja Occidentalis Leafy Twig.

Product ID50845-0184_5d363fa5-e933-4f5a-b750-194102641df4
NDC50845-0184
Product TypeHuman Otc Drug
Proprietary NameUnique Pain Reduction Arthritis
Generic NameAconitum Napellus, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Colchicum Autumnale, Eupatorium Perfoliatum, Guaiacum, Hypericum Perforatum, Ledum Palustre, Mercurius Corrosivus, Rhus Tox, Thuja Occidentalis
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2015-12-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameLiddell Laboratories, Inc.
Substance NameACONITUM NAPELLUS; APIS MELLIFERA; BENZOIC ACID; SUS SCROFA CARTILAGE; COLCHICUM AUTUMNALE BULB; EUPATORIUM PERFOLIATUM FLOWERING TOP; GUAIACUM OFFICINALE RESIN; HYPERICUM PERFORATUM; LEDUM PALUSTRE TWIG; MERCURIC CHLORIDE; TOXICODENDRON PUBESCENS LEAF; THUJA OCCIDENTALIS LEAFY TWIG
Active Ingredient Strength200 [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50845-0184-1

30 mL in 1 BOTTLE, DROPPER (50845-0184-1)
Marketing Start Date2015-12-10
Marketing End Date2022-01-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50845-0184-1 [50845018401]

Unique Pain Reduction Arthritis LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-10
Inactivation Date2020-01-31

Drug Details


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