Natural Relief Arthritis Therapy

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: Natural Relief Arthritis Therapy
Generic name: APIS MELLIFERA, SALICYLIC ACID, RUTA GRAVEOLENS, TOXICODENDRON PUBESCEN, LITHIUM CARBONATE, BRYONIA ALBA, CALCIUM FLUORIDE
Manufacturer: TRP Company
Product type: HUMAN OTC DRUG
SPL set ID: 436f7af7-859e-f7af-e063-6294a90af508
SPL ID: 436f7b11-402d-70e2-e063-6394a90a396f
Version: 1
Effective date: 2025-11-12
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 05:26:29

Harmonized routes table
Harmonized routes
ORAL

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Natural Relief Arthritis Therapy	openfda.brand_name
generic name		APIS MELLIFERA, SALICYLIC ACID, RUTA GRAVEOLENS, TOXICODENDRON PUBESCEN, LITHIUM CARBONATE, BRYONIA ALBA, CALCIUM FLUORIDE	openfda.generic_name
manufacturer name		TRP Company	openfda.manufacturer_name
ndc	package	17312-437-14	openfda.package_ndc
ndc	product	17312-437	openfda.product_ndc
ndc11	package	17312043714	derived:openfda.package_ndc
spl id		436f7b11-402d-70e2-e063-6394a90a396f	id
spl set id		436f7af7-859e-f7af-e063-6294a90af508	set_id
unii		O3B55K4YKI	openfda.unii
unii		O414PZ4LPZ	openfda.unii
unii		N94C2U587S	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		2BMD2GNA4V	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 A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. This product is intended to complement, not replace, standard medical treatment. Initial worsening of symptoms may occur. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if: You experience worsening of symptoms. Symptoms last longer than 7 days.

Reported adverse events (FAERS/openFDA)#

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