Home FDA labels 4044c51d-4d7d-881e-e063-6394a90a9927 Topricin 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 Topricin
Generic name AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLADONNA, CALENDULA OFFICINALIS, CROTALUS HORRIDUS, ECHINACEA, GRAPHITES, HELODERMA HORRIDUM, LACHESIS MUTUS, NAJA TRIPUDIANS, PHOSPHORUS, RHUS TOXICODENDRON, RUTA GRAVEOLENS, SULFUR
Manufacturer Topical BioMedics, Inc.
Product type HUMAN OTC DRUG
SPL set ID 321e83de-71e8-20b4-e054-00144ff8d46c
SPL ID 4044c51d-4d7d-881e-e063-6394a90a9927
Version 4
Effective date 2025-10-03
Source export date 2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:46:37 Harmonized routes table Harmonized routes TOPICAL
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 · 32 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Topricin openfda.brand_name generic name AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLADONNA, CALENDULA OFFICINALIS, CROTALUS HORRIDUS, ECHINACEA, GRAPHITES, HELODERMA HORRIDUM, LACHESIS MUTUS, NAJA TRIPUDIANS, PHOSPHORUS, RHUS TOXICODENDRON, RUTA GRAVEOLENS, SULFUR openfda.generic_name manufacturer name Topical BioMedics, Inc. openfda.manufacturer_name ndc package 61500-5547-1 openfda.package_ndc ndc package 61500-5547-4 openfda.package_ndc ndc package 61500-5547-2 openfda.package_ndc ndc package 61500-5547-9 openfda.package_ndc ndc package 61500-5547-0 openfda.package_ndc ndc package 61500-5547-8 openfda.package_ndc ndc product 61500-5547 openfda.product_ndc ndc11 package 61500554701 derived:openfda.package_ndc ndc11 package 61500554702 derived:openfda.package_ndc ndc11 package 61500554704 derived:openfda.package_ndc ndc11 package 61500554709 derived:openfda.package_ndc ndc11 package 61500554708 derived:openfda.package_ndc ndc11 package 61500554700 derived:openfda.package_ndc spl id 4044c51d-4d7d-881e-e063-6394a90a9927 id spl set id 321e83de-71e8-20b4-e054-00144ff8d46c set_id unii 27YLU75U4W openfda.unii unii KK0Z92II8M openfda.unii unii O80TY208ZW openfda.unii unii 4QQN74LH4O openfda.unii unii 18E7415PXQ openfda.unii unii O9M1UQ4YIO openfda.unii unii N94C2U587S openfda.unii unii 6IO182RP7A openfda.unii unii VB06AV5US8 openfda.unii unii WQZ3G9PF0H openfda.unii unii 70FD1KFU70 openfda.unii unii VSW71SS07I openfda.unii unii ZZ4AG7L7VM openfda.unii unii YHA2XLJ956 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 For external use only. Do not apply in eyes. Ask doctor or pharmacist before using if you are taking prescription medication. Ask a doctor before using if you are pregnant or nursing. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Use only as directed. See doctor if pain persists for more than 3 days or worsens, new symptoms occur, redness or swelling are present because these could be signs of a more serious condition. Before considering any self help regimen always consult your doctor, especially if you are taking a prescription medication.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.