Home FDA labels 41495342-1a27-08cd-e063-6294a90a41b1 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, CROTALUS HORRIDUS, ECHINACEA, GRAPHITES, HELODERMA, LACHESIS MUTUS, NAJA TRIPUDIANS, RHUS TOXICODENDRON, RUTA GRAVEOLENS
Manufacturer Topical BioMedics, Inc.
Product type HUMAN OTC DRUG
SPL set ID 53f5778f-ab62-4dda-9bd9-8cc7fdd69d1e
SPL ID 41495342-1a27-08cd-e063-6294a90a41b1
Version 6
Effective date 2025-10-01
Source export date 2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:37:20 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 · 31 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Topricin openfda.brand_name generic name AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLADONNA, CROTALUS HORRIDUS, ECHINACEA, GRAPHITES, HELODERMA, LACHESIS MUTUS, NAJA TRIPUDIANS, RHUS TOXICODENDRON, RUTA GRAVEOLENS openfda.generic_name manufacturer name Topical BioMedics, Inc. openfda.manufacturer_name ndc package 61500-5527-4 openfda.package_ndc ndc package 61500-5527-6 openfda.package_ndc ndc package 61500-5527-2 openfda.package_ndc ndc package 61500-5527-1 openfda.package_ndc ndc package 61500-5527-3 openfda.package_ndc ndc package 61500-5527-5 openfda.package_ndc ndc package 61500-5527-8 openfda.package_ndc ndc product 61500-5527 openfda.product_ndc ndc11 package 61500552703 derived:openfda.package_ndc ndc11 package 61500552701 derived:openfda.package_ndc ndc11 package 61500552706 derived:openfda.package_ndc ndc11 package 61500552704 derived:openfda.package_ndc ndc11 package 61500552708 derived:openfda.package_ndc ndc11 package 61500552705 derived:openfda.package_ndc ndc11 package 61500552702 derived:openfda.package_ndc spl id 41495342-1a27-08cd-e063-6294a90a41b1 id spl set id 53f5778f-ab62-4dda-9bd9-8cc7fdd69d1e set_id unii KK0Z92II8M openfda.unii unii O80TY208ZW openfda.unii unii 4QQN74LH4O openfda.unii unii O9M1UQ4YIO openfda.unii unii N94C2U587S openfda.unii unii 6IO182RP7A openfda.unii unii VB06AV5US8 openfda.unii unii WQZ3G9PF0H 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 a presciption medication. Ask doctor or pharmacist before using if you are pregnant or nursing. Keep all medicines out of reach of children . Use only as directed, see doctor if pain persists for more than 3 days or worsens, if new symptoms occur, or if 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 prescription medication.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.