FDA.reportPublic FDA data

NativeRemedies® Arthritis Ease Tablets

Manufacturer
Silver Star Brands | OHM Pharma, Inc.
Effective date
2025-01-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:30:00

Label at a glance#

ProductArthritis Ease
Active ingredientBENZOIC ACID, BRYONIA ALBA ROOT, ARNICA MONTANA, TOXICODENDRON RADICANS LEAF, CALCIUM PHOSPHATE, COLCHICUM AUTUMNALE BULB, RUTA GRAVEOLENS FLOWERING TOP
Label structure10 sections

Indications and uses

Uses*: Homeopathic relief from symptoms of minor arthritis pain. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

Directions: Chew or dissolve tablets in the mouth. For Adults and Children 12+: Take 2 tablets every 15-20 minutes up to 4 doses, then every 4 hours until symptoms subside.

Label contents#

Full prescribing information#

HPUS Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

HPUS Active Ingredients: Equal volumes of each ingredient ina 12C potency: Arnica, Benzoicum ac, Bryonia, Calc phos, Colchicum, Rhus tox, Ruta.

Uses*

INDICATIONS & USAGE SECTION

Uses*: Homeopathic relief from symptoms of minor arthritis pain.

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS SECTION

Warnings: If symptoms persist or worsen, consult a healthcare professional. Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: Chew or dissolve tablets in the mouth. For Adults and Children 12+: Take 2 tablets every 15-20 minutes up to 4 doses, then every 4 hours until symptoms subside.

OTHER SAFETY INFORMATION

Contains no artificial flavors or colorants. No gluten added. Lactose-free.

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Magnesium Stearate, Maltodextrin, Sucrose.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medication out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - PURPOSE SECTION

Temporarily relieves symptoms of minor arthritis pain*

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Arthritis Ease labelArthritis Ease label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68703-376-802023-12-26C16284748780-1f386c649-d339-0266-e053-dadaa90a7c1aNativeRemedies® Arthritis Ease Tablets
68703-376-802023-01-30C16284748780-1f386c649-d339-0266-e053-dadaa90a7c1aNativeRemedies® Arthritis Ease Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68703-376-80Arthritis Ease180 in 1 BOTTLE, GLASSTABLET1804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68703-376ARTHRITIS EASE (ARNICA, BENZOICUM AC, BRYONIA, CALC PHOS, COLCHIUM, RHUS TOX, RUTA) TABLET [SILVER STAR BRANDS]4Current NDC, Legacy NDC, 1 package rows20250103_c68b587f-14eb-395a-e053-2a95a90ae801.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68703-37668703-376-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZOIC ACID8SKN0B0MIMACTIB
SUCROSEC151H8M554IACT
BRYONIA ALBA ROOTT7J046YI2BACTIB
ARNICA MONTANAO80TY208ZWACTIB
TOXICODENDRON RADICANS LEAFCDH3461U7LACTIB
MAGNESIUM STEARATE70097M6I30IACT
CALCIUM PHOSPHATE97Z1WI3NDXACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
RUTA GRAVEOLENS FLOWERING TOPN94C2U587SACTIB
MALTODEXTRIN7CVR7L4A2DIACT

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
Arthritis EaseARNICA, BENZOICUM AC, BRYONIA, CALC PHOS, COLCHIUM, RHUS TOX, RUTASilver Star Brandsc68b587f-14eb-395a-e053-2a95a90ae8012025-01-01WarningsExact identifier
ndc (package): 68703-376-80
ndc (product): 68703-376
ndc11 (package): 68703037680
spl id: 2ab0eabe-29c4-5582-e063-6394a90aa251
spl set id: c68b587f-14eb-395a-e053-2a95a90ae801

Reported adverse events (FAERS/openFDA)#

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