Home DailyMed 2ae11146-b869-4a53-afa3-805de12921f9 Back Pain and Sciatica Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Liddell Laboratories, Inc. | Apotheca Company
Effective date 2024-07-01
Label type HUMAN OTC DRUG LABEL
Version 4
Source full-release
Hydrated at 2026-06-01 02:27:27 Label at a glance# Product Back Pain and Sciatica
Active ingredient ACONITUM NAPELLUS WHOLE, ARNICA MONTANA WHOLE, ATROPA BELLADONNA, BLACK COHOSH, EUPHORBIA RESINIFERA RESIN, GELSEMIUM SEMPERVIRENS ROOT, PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE, HYPERICUM PERFORATUM WHOLE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PHYTOLACCA AMERICANA ROOT, RANUNCULUS BULBOSUS WHOLE, TOXICODENDRON PUBESCENS LEAF
Label structure 9 sections
Indications and uses May temporarily relieve these symptoms of back pain and sciatica: lower back pain muscle cramps neck and back stiffness muscle spasms** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dosage and administration Adults and children over 12: Spray twice under the tongue three times per day. For severe symptoms, dosage may be taken up to six times the first day. Children 12 and under: Consult a doctor prior to use.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50845-0237-1 Back Pain and Sciatica 30 mL in 1 BOTTLE, SPRAY SPRAY 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50845-0237 BACK PAIN AND SCIATICA (ACONITUM NAPELLUS, ARNICA MONTANA, BELLADONNA, CIMICIFUGA RACEMOSA, EUPHORBIUM OFFICINARUM, GELSEMIUM SEMPERVIRENS, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PHYTOLACCA DECANDRA, RANUNCULUS BULBOSUS, RHUS TOX) SPRAY [LIDDELL LABORATORIES, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20240702_2ae11146-b869-4a53-afa3-805de12921f9.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 22 matching rows.
Back Pain and Sciatica Aconitum Napellus, Arnica Montana, Belladonna, Cimicifuga Racemosa, Euphorbium Officinarum, Gelsemium Sempervirens, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox ACONITUM NAPELLUS WHOLE ACONITUM NAPELLUS ARNICA MONTANA WHOLE ARNICA MONTANA ATROPA BELLADONNA BLACK COHOSH EUPHORBIA RESINIFERA RESIN GELSEMIUM SEMPERVIRENS ROOT PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE PSEUDOGNAPHALIUM OBTUSIFOLIUM HYPERICUM PERFORATUM WHOLE HYPERICUM PERFORATUM MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION PHYTOLACCA AMERICANA ROOT RANUNCULUS BULBOSUS WHOLE RANUNCULUS BULBOSUS TOXICODENDRON PUBESCENS LEAF WATER ALCOHOL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 14 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Back Pain and Sciatica ACONITUM NAPELLUS, ARNICA MONTANA, BELLADONNA, CIMICIFUGA RACEMOSA, EUPHORBIUM OFFICINARUM, GELSEMIUM SEMPERVIRENS, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PHYTOLACCA DECANDRA, RANUNCULUS BULBOSUS, RHUS TOX Liddell Laboratories, Inc. 2ae11146-b869-4a53-afa3-805de12921f9 2024-07-01 Warnings Exact identifier ndc (package): 50845-0237-1 ndc (product): 50845-0237 ndc11 (package): 50845023701 spl id: d340d01b-3f0f-4863-a0b0-94cff53d2215 spl set id: 2ae11146-b869-4a53-afa3-805de12921f9
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.