Leg and Back Pain Relief

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: Leg and Back Pain Relief
Generic name: CAPSICUM ANNUUM, COLOCYNTHIS, GNAPHALIUM POLYCEPHALUM, MAGNESIA PHOSPHORICA
Manufacturer: The Magni Company
Product type: HUMAN OTC DRUG
SPL set ID: ef30c7cf-6da0-424d-8737-c968436768fd
SPL ID: bc3ebce9-dde9-4bde-8568-878ab1c5be26
Version: 4
Effective date: 2026-04-22
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 05:26:36

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Leg and Back Pain Relief	openfda.brand_name
generic name		CAPSICUM ANNUUM, COLOCYNTHIS, GNAPHALIUM POLYCEPHALUM, MAGNESIA PHOSPHORICA	openfda.generic_name
manufacturer name		The Magni Company	openfda.manufacturer_name
ndc	package	43689-0013-2	openfda.package_ndc
ndc	package	43689-0013-1	openfda.package_ndc
ndc	product	43689-0013	openfda.product_ndc
ndc11	package	43689001301	derived:openfda.package_ndc
ndc11	package	43689001302	derived:openfda.package_ndc
spl id		bc3ebce9-dde9-4bde-8568-878ab1c5be26	id
spl set id		ef30c7cf-6da0-424d-8737-c968436768fd	set_id
unii		00UK7646FG	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		36XQ854NWW	openfda.unii
unii		23H32AOH17	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: • If pregnant or breastfeeding, ask a health professional before use • Keep out of reach of children • Do not take this product for pain for more than 7 days unless directed by a doctor. • If pain persists or gets worse, if new symptoms occur, or if redness or swelling is present, consult a doctor because these could be signs of a serious condition. • In case of overdose, get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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