Pain and Fatigue 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: Pain and Fatigue Relief
Generic name: ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CONIINUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI BICHROMICUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, URICUM ACIDUM
Manufacturer: The Magni Company
Product type: HUMAN OTC DRUG
SPL set ID: 7c689153-2002-421d-b573-76b0052550e0
SPL ID: ec83ed89-ee4e-408e-8dcf-244a762a5e9b
Version: 5
Effective date: 2023-01-26
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:44

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Pain and Fatigue Relief	openfda.brand_name
generic name		ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CONIINUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI BICHROMICUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, URICUM ACIDUM	openfda.generic_name
manufacturer name		The Magni Company	openfda.manufacturer_name
ndc	package	43689-0015-2	openfda.package_ndc
ndc	package	43689-0015-1	openfda.package_ndc
ndc	product	43689-0015	openfda.product_ndc
ndc11	package	43689001501	derived:openfda.package_ndc
ndc11	package	43689001502	derived:openfda.package_ndc
spl id		ec83ed89-ee4e-408e-8dcf-244a762a5e9b	id
spl set id		7c689153-2002-421d-b573-76b0052550e0	set_id
unii		268B43MJ25	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		C479P32L2D	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		3B8D35Y7S4	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		T4423S18FM	openfda.unii
unii		E4GA8884NN	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. In case of overdose, get medical help or contact a Poison Control Center right away • If symptoms persist for more than 7 days or worsen, consult your physician

Reported adverse events (FAERS/openFDA)#

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