Home FDA labels f44b45b5-cfa8-4d2d-a530-f973032c08d1 HEADACHE HP 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 HEADACHE HP
Generic name SILVER NITRATE, ATROPA BELLADONNA, BRYONIA ALBA ROOT, GELSEMIUM SEMPERVIRENS ROOT, NITROGLYCERIN, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MELILOTUS OFFICINALIS TOP, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, SILICON DIOXIDE, SPIGELIA ANTHELMIA
Manufacturer Natural Creations, Inc.
Product type HUMAN OTC DRUG
SPL set ID c38b83f0-3918-4ef6-8dfd-48fe438e584a
SPL ID f44b45b5-cfa8-4d2d-a530-f973032c08d1
Version 3
Effective date 2025-12-12
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:29:03 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 · 19 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name HEADACHE HP openfda.brand_name generic name SILVER NITRATE, ATROPA BELLADONNA, BRYONIA ALBA ROOT, GELSEMIUM SEMPERVIRENS ROOT, NITROGLYCERIN, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MELILOTUS OFFICINALIS TOP, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, SILICON DIOXIDE, SPIGELIA ANTHELMIA openfda.generic_name manufacturer name Natural Creations, Inc. openfda.manufacturer_name ndc package 43406-0025-1 openfda.package_ndc ndc product 43406-0025 openfda.product_ndc ndc11 package 43406002501 derived:openfda.package_ndc spl id f44b45b5-cfa8-4d2d-a530-f973032c08d1 id spl set id c38b83f0-3918-4ef6-8dfd-48fe438e584a set_id unii 269XH13919 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 95IT3W8JZE openfda.unii unii 451W47IQ8X openfda.unii unii WYT05213GE openfda.unii unii GM6P02J2DX openfda.unii unii WQZ3G9PF0H openfda.unii unii T7J046YI2B openfda.unii unii VSW71SS07I openfda.unii unii G59M7S0WS3 openfda.unii unii C88X29Y479 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 WARNING : Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN . In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. DO not use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.