GUNA PAIN MANAGEMENT

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: GUNA PAIN MANAGEMENT
Generic name: ACHILLEA MILLEFOLIUM WHOLE - BELLIS PERENNIS WHOLE - MATRICARIA CHAMOMILLA WHOLE - TOXICODENDRON PUBESCENS WHOLE - RUTA GRAVEOLENS FLOWERING TOP - COMFREY ROOT - APIS MELLIFERA - BRYONIA ALBA ROOT - HISTAMINE HYDROCHLORIDE - HYPERICUM PERFORATUM - KALMIA LATIFOLIA LEAF - ARNICA MONTANA WHOLE - PORK LIVER -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: af5bad63-6d57-2260-e053-2995a90afb7e
SPL ID: af5b9acf-ede8-0899-e053-2a95a90a1706
Version: 1
Effective date: 2020-09-15
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:44

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		GUNA PAIN MANAGEMENT	openfda.brand_name
generic name		ACHILLEA MILLEFOLIUM WHOLE - BELLIS PERENNIS WHOLE - MATRICARIA CHAMOMILLA WHOLE - TOXICODENDRON PUBESCENS WHOLE - RUTA GRAVEOLENS FLOWERING TOP - COMFREY ROOT - APIS MELLIFERA - BRYONIA ALBA ROOT - HISTAMINE HYDROCHLORIDE - HYPERICUM PERFORATUM - KALMIA LATIFOLIA LEAF - ARNICA MONTANA WHOLE - PORK LIVER -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-465-18	openfda.package_ndc
ndc	product	17089-465	openfda.product_ndc
ndc11	package	17089046518	derived:openfda.package_ndc
spl id		af5b9acf-ede8-0899-e053-2a95a90a1706	id
spl set id		af5bad63-6d57-2260-e053-2995a90afb7e	set_id
unii		2FXJ6SW4PK	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		3POA0Q644U	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		79N6542N18	openfda.unii
unii		2HU33I03UY	openfda.unii
unii		N94C2U587S	openfda.unii
unii		M9VVZ08EKQ	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		6EC706HI7F	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 Stop use and ask doctor if symptoms worsen or persist more than 5 days. If pregnant or breast-feeding ask a health care professional before use. Keep out of reach of children. In case of accidental overdose, seek professional assistance or contact a poison control center immediately Contains ethyl alcohol 30%

Reported adverse events (FAERS/openFDA)#

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