Home FDA labels d44a0c64-228a-9c8f-e053-2a95a90a2bbf Arnica Well 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 Arnica Well
Generic name BELLIS PERENNIS, CALENDULA OFFICINALIS, HAMAMELIS VIRGINIANA, MILLEFOLLIUM MT, CHAMOMILLA, FERRUM PHOSPHORICUM, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, APIS MELLIFICA, ARNICA MONTANA, BELLADONNA, SYMPHYTUM OFFICINALE, HYPERICUM PERFORATUM.
Manufacturer Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics 052584997
Product type HUMAN OTC DRUG
SPL set ID 52647581-e65c-4f43-bb61-600174bc8e7e
SPL ID d44a0c64-228a-9c8f-e053-2a95a90a2bbf
Version 4
Effective date 2021-12-29
Source export date 2026-09-28
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:26:32 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Arnica Well openfda.brand_name generic name BELLIS PERENNIS, CALENDULA OFFICINALIS, HAMAMELIS VIRGINIANA, MILLEFOLLIUM MT, CHAMOMILLA, FERRUM PHOSPHORICUM, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, APIS MELLIFICA, ARNICA MONTANA, BELLADONNA, SYMPHYTUM OFFICINALE, HYPERICUM PERFORATUM. openfda.generic_name manufacturer name Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics 052584997 openfda.manufacturer_name ndc package 66492-069-02 openfda.package_ndc ndc package 66492-069-03 openfda.package_ndc ndc product 66492-069 openfda.product_ndc ndc11 package 66492006902 derived:openfda.package_ndc ndc11 package 66492006903 derived:openfda.package_ndc spl id d44a0c64-228a-9c8f-e053-2a95a90a2bbf id spl set id 52647581-e65c-4f43-bb61-600174bc8e7e set_id unii 2FXJ6SW4PK openfda.unii unii 877L01IZ0P openfda.unii unii XK4IUX8MNB openfda.unii unii O80TY208ZW openfda.unii unii 18E7415PXQ openfda.unii unii 2HU33I03UY openfda.unii unii HF539G9L3Q openfda.unii unii M9VVZ08EKQ openfda.unii unii 91GQH8I5F7 openfda.unii unii WQZ3G9PF0H openfda.unii unii 7S82P3R43Z openfda.unii unii G0R4UBI2ZZ openfda.unii unii T7S323PKJS 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 TOPICAL USE ONLY. DO NOT APPLY ON OPEN WOUNDS. Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. IF PAIN PERSISTS, seek the advice of your health care professional. KEEP OUT OF THE REACH OF CHILDREN.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.