Home FDA labels a12452f8-d7ea-4e84-b827-7483e69b5f48 EMF 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 EMF
Generic name ARGENTUM NITRICUM, ARNICA MONTANA, BAPTISIA TINCTORIA, CINCHONA OFFICINALIS, GALIUM APARINE, HEPAR SUIS, NATRUM CARBONICUM, PANAX GINSENG, PHOSPHORICUM ACIDUM, PHOSPHORUS, RHODODENDRON CHRYSANTHUM, STRONTIUM CARBONICUM, SULPHUR IODATUM, THUJA OCCIDENTALIS, X-RAY
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 3fa1b8d3-7c09-431b-b843-03b2ef8a92b1
SPL ID a12452f8-d7ea-4e84-b827-7483e69b5f48
Version 4
Effective date 2024-07-01
Source export date 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:51 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name EMF openfda.brand_name generic name ARGENTUM NITRICUM, ARNICA MONTANA, BAPTISIA TINCTORIA, CINCHONA OFFICINALIS, GALIUM APARINE, HEPAR SUIS, NATRUM CARBONICUM, PANAX GINSENG, PHOSPHORICUM ACIDUM, PHOSPHORUS, RHODODENDRON CHRYSANTHUM, STRONTIUM CARBONICUM, SULPHUR IODATUM, THUJA OCCIDENTALIS, X-RAY openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0248-1 openfda.package_ndc ndc product 50845-0248 openfda.product_ndc ndc11 package 50845024801 derived:openfda.package_ndc spl id a12452f8-d7ea-4e84-b827-7483e69b5f48 id spl set id 3fa1b8d3-7c09-431b-b843-03b2ef8a92b1 set_id unii 27YLU75U4W openfda.unii unii O80TY208ZW openfda.unii unii CUQ3A77YXI openfda.unii unii 1NT28V9397 openfda.unii unii 95IT3W8JZE openfda.unii unii IV92NQJ73U openfda.unii unii 6PRJ93602P openfda.unii unii S003A158SB openfda.unii unii E4GA8884NN openfda.unii unii 45P3261C7T openfda.unii unii 5EF0HWI5WU openfda.unii unii Z4B6561488 openfda.unii unii 41YPU4MMCA openfda.unii unii 6EC706HI7F openfda.unii unii L6L8KA2AA0 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 doctor before using product. 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.