FDA.reportPublic FDA data

Natural Relief Arthritis Therapy

Product NDC
17312-437
11-digit product format
173120437
Labeler code
17312
Product ID
17312-437_436f7b11-402d-70e2-e063-6394a90a396f
Type
HUMAN OTC DRUG
Nonproprietary name
APIS MELLIFERA, SALICYLIC ACID, RUTA GRAVEOLENS, TOXICODENDRON PUBESCEN, LITHIUM CARBONATE, BRYONIA ALBA, CALCIUM FLUORIDE
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
TRP Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2025-04-30
Substance
APIS MELLIFERA; BRYONIA ALBA ROOT; CALCIUM FLUORIDE; LITHIUM CARBONATE; RUTA GRAVEOLENS FLOWERING TOP; SALICYLIC ACID; TOXICODENDRON PUBESCENS LEAF
Active strength
6; 6; 10; 6; 6; 3; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Mood Stabilizer [EPC], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Natural Relief Arthritis Therapy
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
APIS MELLIFERA6 [hp_X]/1
BRYONIA ALBA ROOT6 [hp_X]/1
CALCIUM FLUORIDE10 [hp_X]/1
LITHIUM CARBONATE6 [hp_X]/1
TOXICODENDRON PUBESCENS LEAF6 [hp_X]/1
RUTA GRAVEOLENS FLOWERING TOP3 [hp_X]/1
SALICYLIC ACID6 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7S82P3R43ZInternal UNII lookup
T7J046YI2BInternal UNII lookup
O3B55K4YKIInternal UNII lookup
2BMD2GNA4VInternal UNII lookup
6IO182RP7AInternal UNII lookup
N94C2U587SInternal UNII lookup
O414PZ4LPZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
436f7af7-859e-f7af-e063-6294a90af508Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
a62a50ac-1535-4461-9768-8ae703e2e9fbProduct name120210525
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
bc07ef78-e82d-0c19-31f4-31f263780582Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17312-437-14Natural Relief Arthritis Therapy70 in 1 BOTTLETABLET, ORALLY DISINTEGRATING701
17312-437-14Natural Relief Arthritis Therapy1 in 1 PACKAGETABLET, ORALLY DISINTEGRATING11

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
Natural Relief Arthritis TherapyAPIS MELLIFERA, SALICYLIC ACID, RUTA GRAVEOLENS, TOXICODENDRON PUBESCEN, LITHIUM CARBONATE, BRYONIA ALBA, CALCIUM FLUORIDETRP Company436f7af7-859e-f7af-e063-6294a90af5082025-11-12WarningsExact identifier
ndc (product): 17312-437

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
17312-437-14173120437141 BOTTLE in 1 PACKAGE (17312-437-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE1 bottle2025-04-30NoNoCurrent