Home DailyMed e53db678-6924-41b6-ad7e-32e40d7ee785 Inflammation Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Deseret Biologicals, Inc. | Apotheca Company
Effective date 2024-04-08
Label type HUMAN OTC DRUG LABEL
Version 1
Source full-release
Hydrated at 2026-06-01 02:26:35 Label at a glance# Product Inflammation
Active ingredient APIS MELLIFERA, ARNICA MONTANA WHOLE, BAPTISIA TINCTORIA ROOT, BENZOIC ACID, BRYONIA ALBA ROOT, COLCHICUM AUTUMNALE BULB, SOLANUM DULCAMARA TOP, ECHINACEA ANGUSTIFOLIA WHOLE, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, MERCURIALIS PERENNIS WHOLE, TOXICODENDRON PUBESCENS LEAF, SOLANUM NIGRUM WHOLE
Label structure 9 sections
Indications and uses • For the temporary relief of symptoms including: • inflammation • inflamed joints • painful joints • stiff joints • muscle pain • headache • cough • fever These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Dosage and administration 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-2112-1 Inflammation 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-2112 INFLAMMATION (APIS MELLIFICA, ARNICA MONTANA, BAPTISIA TINCTORIA, BENZOICUM ACIDUM, BRYONIA (ALBA), COLCHICUM AUTUMNALE, DULCAMARA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, EUPATORIUM PERFOLIATUM, MERCURIALIS PERENNIS, RHUS TOX, SOLANUM NIGRUM) LIQUID [DESERET BIOLOGICALS, INC.] 1 Current NDC, 1 package rows 20240410_e53db678-6924-41b6-ad7e-32e40d7ee785.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 20 matching rows.
Inflammation Apis Mellifica, Arnica Montana, Baptisia Tinctoria, Benzoicum Acidum, Bryonia (Alba), Colchicum Autumnale, Dulcamara, Echinacea (Angustifolia), Eucalyptus Globulus, Eupatorium Perfoliatum, Mercurialis Perennis, Rhus Tox, Solanum Nigrum APIS MELLIFERA ARNICA MONTANA WHOLE ARNICA MONTANA BAPTISIA TINCTORIA ROOT BENZOIC ACID BRYONIA ALBA ROOT COLCHICUM AUTUMNALE BULB SOLANUM DULCAMARA TOP ECHINACEA ANGUSTIFOLIA WHOLE ECHINACEA ANGUSTIFOLIA EUCALYPTUS GLOBULUS LEAF EUPATORIUM PERFOLIATUM FLOWERING TOP MERCURIALIS PERENNIS WHOLE MERCURIALIS PERENNIS TOXICODENDRON PUBESCENS LEAF SOLANUM NIGRUM WHOLE WATER ALCOHOL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 15 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Inflammation APIS MELLIFICA, ARNICA MONTANA, BAPTISIA TINCTORIA, BENZOICUM ACIDUM, BRYONIA (ALBA), COLCHICUM AUTUMNALE, DULCAMARA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, EUPATORIUM PERFOLIATUM, MERCURIALIS PERENNIS, RHUS TOX, SOLANUM NIGRUM Deseret Biologicals, Inc. e53db678-6924-41b6-ad7e-32e40d7ee785 2024-04-08 Warnings Exact identifier ndc (package): 43742-2112-1 ndc (product): 43742-2112 ndc11 (package): 43742211201 spl id: bdfd4d37-8af9-40a8-bb69-8eb95c1c1024 spl set id: e53db678-6924-41b6-ad7e-32e40d7ee785
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.