Home FDA labels da438549-da2d-46d4-8cb1-bbe4bb636088 Tension Headache 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 Tension Headache
Generic name ACONITUM NAPELLUS, CARDUUS MARIANUS, COFFEA CRUDA, DIOSCOREA VILLOSA, GELSEMIUM SEMPERVIRENS, GNAPHALIUM POLYCEPHALUM, IRIS VERSICOLOR, PASSIFLORA INCARNATA, STELLARIA MEDIA, VERBASCUM THAPSUS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 897a3348-4d9d-4f74-a330-d6492baa4d03
SPL ID da438549-da2d-46d4-8cb1-bbe4bb636088
Version 2
Effective date 2025-11-20
Source export date 2026-09-28
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:37:16 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Tension Headache openfda.brand_name generic name ACONITUM NAPELLUS, CARDUUS MARIANUS, COFFEA CRUDA, DIOSCOREA VILLOSA, GELSEMIUM SEMPERVIRENS, GNAPHALIUM POLYCEPHALUM, IRIS VERSICOLOR, PASSIFLORA INCARNATA, STELLARIA MEDIA, VERBASCUM THAPSUS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0282-2 openfda.package_ndc ndc package 50845-0282-1 openfda.package_ndc ndc product 50845-0282 openfda.product_ndc ndc11 package 50845028202 derived:openfda.package_ndc ndc11 package 50845028201 derived:openfda.package_ndc spl id da438549-da2d-46d4-8cb1-bbe4bb636088 id spl set id 897a3348-4d9d-4f74-a330-d6492baa4d03 set_id unii IWY3IWX2G8 openfda.unii unii 3SW678MX72 openfda.unii unii 2H03479QVR openfda.unii unii C9TD27U172 openfda.unii unii 639KR60Q1Q openfda.unii unii U946SH95EE openfda.unii unii 36XQ854NWW openfda.unii unii U0NQ8555JD openfda.unii unii CLF5YFS11O openfda.unii unii X43D4L3DQC 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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a health professional before use. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken. Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.