Home FDA labels 98ae5431-1b62-4394-a9b9-cb8c45f674f2 Pain openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Pain
Generic name ACONITUM NAPELLUS, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA (ALBA), CARTILAGO SUIS, CAUSTICUM, CHAMOMILLA, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, PYROGENIUM, RANUNCULUS BULBOSUS, SYMPHYTUM OFFICINALE
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID b591e679-b481-47f1-8d4e-3f3040e9a42a
SPL ID 98ae5431-1b62-4394-a9b9-cb8c45f674f2
Version 2
Effective date 2023-12-19
Source export date 2026-10-12
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:44:55 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Pain openfda.brand_name generic name ACONITUM NAPELLUS, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA (ALBA), CARTILAGO SUIS, CAUSTICUM, CHAMOMILLA, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, PYROGENIUM, RANUNCULUS BULBOSUS, SYMPHYTUM OFFICINALE openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0265-1 openfda.package_ndc ndc product 50845-0265 openfda.product_ndc ndc11 package 50845026501 derived:openfda.package_ndc spl id 98ae5431-1b62-4394-a9b9-cb8c45f674f2 id spl set id b591e679-b481-47f1-8d4e-3f3040e9a42a set_id unii XK4IUX8MNB openfda.unii unii 3SW678MX72 openfda.unii unii DD5FO1WKFU openfda.unii unii O80TY208ZW openfda.unii unii 2HU33I03UY openfda.unii unii 1TI1O9028K openfda.unii unii 29SUH5R3HU openfda.unii unii HF539G9L3Q openfda.unii unii M9VVZ08EKQ openfda.unii unii 73ECW5WG2F openfda.unii unii AEQ8NXJ0MB openfda.unii unii T7J046YI2B openfda.unii unii 36XQ854NWW openfda.unii unii U0NQ8555JD openfda.unii unii CLF5YFS11O openfda.unii unii G0R4UBI2ZZ openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: If symptoms persist for more than 7 days, consult a doctor. If pregnant or breast feeding, ask a doctor before use. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.