GUNA-PMS

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-PMS
Generic name: ARSENIC TRIOXIDE - ESTRADIOL - GOLDENSEAL - LACHESIS MUTA VENOM - MAGNESIUM PHOSPHATE - MATRICARIA RECUTITA - MELATONIN - PROGESTERONE - STRYCHNOS NUX-VOMICA SEED - SULFUR - SUS SCROFA OVARY - SUS SCROFA PITUITARY GLAND -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: 86f341b1-a8f7-4833-a1be-e51610b05bcd
SPL ID: 7e9133b3-3360-2bd0-e053-2a91aa0a3bf3
Version: 2
Effective date: 2018-12-21
Source export date: 2026-10-27
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2c7d3f7bcea1543046130e07dcbaf7eea5fb0ce23f7faa6458d1c6d80c3fa0c3/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:42:43

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA-PMS	openfda.brand_name
generic name		ARSENIC TRIOXIDE - ESTRADIOL - GOLDENSEAL - LACHESIS MUTA VENOM - MAGNESIUM PHOSPHATE - MATRICARIA RECUTITA - MELATONIN - PROGESTERONE - STRYCHNOS NUX-VOMICA SEED - SULFUR - SUS SCROFA OVARY - SUS SCROFA PITUITARY GLAND -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-290-18	openfda.package_ndc
ndc	product	17089-290	openfda.product_ndc
ndc11	package	17089029018	derived:openfda.package_ndc
spl id		7e9133b3-3360-2bd0-e053-2a91aa0a3bf3	id
spl set id		86f341b1-a8f7-4833-a1be-e51610b05bcd	set_id
unii		269XH13919	openfda.unii
unii		453COF7817	openfda.unii
unii		L0PFEMQ1DT	openfda.unii
unii		S7YTV04R8O	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		4TI98Z838E	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		4G7DS2Q64Y	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		JL5DK93RCL	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 persist more than 5 days. 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. Contains ethyl alcohol 30%

Reported adverse events (FAERS/openFDA)#

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