Home FDA labels 88ac1590-a4a6-425d-a5ed-ba6d3195fe94 Vaccines 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 Vaccines
Generic name ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, MORBILLINUM, NATRUM MURIATICUM, SILICEA, SULPHUR IODATUM, THUJA OCCIDENTALIS, URTICA URENS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 6e6e67d4-089e-4775-b4a4-5511953f6e3f
SPL ID 88ac1590-a4a6-425d-a5ed-ba6d3195fe94
Version 3
Effective date 2024-11-04
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 02:29:11 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 · 17 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Vaccines openfda.brand_name generic name ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, MORBILLINUM, NATRUM MURIATICUM, SILICEA, SULPHUR IODATUM, THUJA OCCIDENTALIS, URTICA URENS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0262-2 openfda.package_ndc ndc product 50845-0262 openfda.product_ndc ndc11 package 50845026202 derived:openfda.package_ndc spl id 88ac1590-a4a6-425d-a5ed-ba6d3195fe94 id spl set id 6e6e67d4-089e-4775-b4a4-5511953f6e3f set_id unii 877L01IZ0P openfda.unii unii XK4IUX8MNB openfda.unii unii HT3R7C012Q openfda.unii unii O80TY208ZW openfda.unii unii 1NT28V9397 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 451W47IQ8X openfda.unii unii IHN2NQ5OF9 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. Ask a doctor before use if excessive redness or swelling is present. Stop use and ask a doctor if symptoms persist for more than 7 days, 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. Other Information: Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.