NDC 63083-2041

Low Back Pain Drops 2041

Low Back Pain Drops

Low Back Pain Drops 2041 is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Professional Complementary Health Formulas. The primary component is Aconitum Napellus Whole; Amaryllis Belladonna Whole; Apis Mellifera; Arnica Montana Whole; Atropine; Berberis Vulgaris Root Bark; Bos Taurus Bone Marrow; Bos Taurus Hypothalamus; Bos Taurus Somatic Nerve; Causticum; Graphite; Hypericum Perforatum Whole; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Potassium Dichromate; Sepia Officinalis Juice; Toxicodendron Pubescens Leaf.

Product ID63083-2041_e2c160bd-1c37-4cce-878c-c56b9156bff4
NDC63083-2041
Product TypeHuman Otc Drug
Proprietary NameLow Back Pain Drops 2041
Generic NameLow Back Pain Drops
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1984-08-15
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameProfessional Complementary Health Formulas
Substance NameACONITUM NAPELLUS WHOLE; AMARYLLIS BELLADONNA WHOLE; APIS MELLIFERA; ARNICA MONTANA WHOLE; ATROPINE; BERBERIS VULGARIS ROOT BARK; BOS TAURUS BONE MARROW; BOS TAURUS HYPOTHALAMUS; BOS TAURUS SOMATIC NERVE; CAUSTICUM; GRAPHITE; HYPERICUM PERFORATUM WHOLE; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; POTASSIUM DICHROMATE; SEPIA OFFICINALIS JUICE; TOXICODENDRON PUBESCENS LEAF
Active Ingredient Strength6 [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
Pharm ClassesAllergens [CS], Anticholinergic [EPC], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63083-2041-2

59 mL in 1 BOTTLE, DROPPER (63083-2041-2)
Marketing Start Date1985-08-15
NDC Exclude FlagN
Sample Package?N

Drug Details


© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.