Home FDA labels 0e92e39f-2391-463b-981e-260d442306b8 Insect Bites 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 Insect Bites
Generic name ANTHRACINUM, APIS MELLIFICA, ARNICA MONTANA, CALENDULA OFFICINALIS, CAMPHORA, CONIUM MACULATUM, ECHINACEA (ANGUSTIFOLIA), GRINDELIA, HISTAMINUM HYDROCHLORICUM, HYPERICUM PERFORATUM, LACHESIS MUTUS, LATRODECTUS MACTANS, LEDUM PALUSTRE, PYROGENIUM, TARENTULA CUBENSIS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID e36fd898-00b4-4b62-8440-f1f1710bb6b4
SPL ID 0e92e39f-2391-463b-981e-260d442306b8
Version 1
Effective date 2024-08-23
Source export date 2026-11-06
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 08:02:55 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Insect Bites openfda.brand_name generic name ANTHRACINUM, APIS MELLIFICA, ARNICA MONTANA, CALENDULA OFFICINALIS, CAMPHORA, CONIUM MACULATUM, ECHINACEA (ANGUSTIFOLIA), GRINDELIA, HISTAMINUM HYDROCHLORICUM, HYPERICUM PERFORATUM, LACHESIS MUTUS, LATRODECTUS MACTANS, LEDUM PALUSTRE, PYROGENIUM, TARENTULA CUBENSIS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0281-1 openfda.package_ndc ndc product 50845-0281 openfda.product_ndc ndc11 package 50845028101 derived:openfda.package_ndc spl id 0e92e39f-2391-463b-981e-260d442306b8 id spl set id e36fd898-00b4-4b62-8440-f1f1710bb6b4 set_id unii 877L01IZ0P openfda.unii unii XK4IUX8MNB openfda.unii unii 3POA0Q644U openfda.unii unii O80TY208ZW openfda.unii unii Q28R5GF371 openfda.unii unii 18E7415PXQ openfda.unii unii 29SUH5R3HU openfda.unii unii 41LZ22DD4N openfda.unii unii XJJ7QA858R openfda.unii unii VB06AV5US8 openfda.unii unii N20HL7Q941 openfda.unii unii 3Y5X6RT823 openfda.unii unii VSW71SS07I openfda.unii unii 7S82P3R43Z openfda.unii unii IDB0NAZ6AI 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 health professional 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.