FDA.reportPublic FDA data

Arthritis Pain Relief

Manufacturer
Beaumont Bio Med
Effective date
2018-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:10:36

Label at a glance#

ProductArthritis Pain Relief
Active ingredientACTAEA CIMICIFUGA ROOT, HORSE CHESTNUT, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA ALBA ROOT, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, CAUSTICUM, BLACK COHOSH, FORMIC ACID, HYPERICUM PERFORATUM, COW MILK, RHODODENDRON TOMENTOSUM LEAFY TWIG, LITHIUM CARBONATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PHOSPHORUS, PHYTOLACCA AMERICANA ROOT, ANEMONE PULSATILLA, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, SALICYLIC ACID, SEPIA OFFICINALIS JUICE, ZINC
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

HPUS active ingredients: Actaea, Aesculus hipp, Arnica, Bellis, Bryonia, Calc carb, Calc fluor, Causticum, Cimicifuga, Formicum acidum, Hypericum, Lac vac, Ledum, Lithium carb, Mag phos, Phos, Phytolacca, Pulsatilla, Rhododendron, Rhus tox, Ruta, Salicylicum ac, Sepia, Zinc met. Equal volumes of each ingredient in 10X, 30X, 100X potencies.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Alcohol @ 20% (v/v), Glycerin @ 8% (v/v), in a pure water base.   

INDICATIONS & USAGE SECTION

Indications: For temporary relief of: symptoms of joint pain, Stiffness & discomfort associated with arthritis.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Hold close to mouth and spray 1 dose (3 complete pump sprays) directly in mouth 4-6 times daily until symptoms improve.
  • Before initial dose, depress pump 4-5 times or until primed.
  • Consult a physician for use in children under 12 years of age.

WARNINGS SECTION

Warnings: Stop use and ask a doctor if symptoms persist or worsen. If pregnant or breast feeding, consult a healthcare professional before use. In case of accidental overdose contact a healthcareprofessional immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of the reach of children.

OTHER SAFETY INFORMATION

Other information: Tamper resistant for your protection. Use only if safety seal is intact.      

OTC - PURPOSE SECTION

For temporary relief of: symptoms of joint pain, stiffness & discomfort associated with arthritis.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58066-7042-72020-01-31C16284748780-19d75b9cf-e954-f424-e053-dadaa90a57ceArthritis Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58066-7042-7Arthritis Pain Relief59.2 mL in 1 BOTTLE, SPRAYLIQUID59.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58066-7042ARTHRITIS PAIN RELIEF (ACTAEA, AESCULUS HIPP, ARNICA, BELLIS, BRYONIA, CALC CARB, CALC FLUOR, CAUSTICUM, CIMICIFUGA, FORMICUM ACIDUM, HYPERICUM, LAC VAC, LEDUM, LITHIUM CARB, MAG PHOS, PHOS, PHYTOLACCA, PULSATILLA, RHODODENDRON, RHUS TOX, RUTA, SALICYLICUM AC, SEPIA, ZINC MET.) LIQUID [BEAUMONT BIO MED]1Legacy NDC, 1 package rows20181221_9e88df67-948d-4326-8c4e-a76bfaabd5cf.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58066-704258066-7042-7

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACTAEA CIMICIFUGA ROOT65J267BAZTACTIB
HORSE CHESTNUT3C18L6RJAZACTIB
ARNICA MONTANAO80TY208ZWACTIB
BELLIS PERENNIS2HU33I03UYACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
CALCIUM FLUORIDEO3B55K4YKIACTIB
CAUSTICUMDD5FO1WKFUACTIB
BLACK COHOSHK73E24S6X9ACTIB
FORMIC ACID0YIW783RG1ACTIB
HYPERICUM PERFORATUMXK4IUX8MNBACTIB
COW MILK917J3173FTACTIB
RHODODENDRON TOMENTOSUM LEAFY TWIG877L01IZ0PACTIB
LITHIUM CARBONATE2BMD2GNA4VACTIB
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATEHF539G9L3QACTIB
PHOSPHORUS27YLU75U4WACTIB
PHYTOLACCA AMERICANA ROOT11E6VI8VEGACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
RHODODENDRON AUREUM LEAFIV92NQJ73UACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
RUTA GRAVEOLENS FLOWERING TOPN94C2U587SACTIB
SALICYLIC ACIDO414PZ4LPZACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
ZINCJ41CSQ7QDSACTIB
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
35e33a13-ed59-4a38-87d8-a338082adda19e88df67-948d-4326-8c4e-a76bfaabd5cf2018-01-01WarningsExact identifier
spl id: 35e33a13-ed59-4a38-87d8-a338082adda1
spl set id: 9e88df67-948d-4326-8c4e-a76bfaabd5cf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.