GUNA OSTEO

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 OSTEO
Generic name: ARNICA MONTANA ROOT - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - EQUISETUM HYEMALE - FUMARIC ACID - SUS SCROFA UMBILICAL CORD - SUS SCROFA OVARY - SUS SCROFA PLACENTA - COMFREY ROOT - SUCCINIC ACID - SILICON DIOXIDE -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: ba4462d6-9751-530f-e053-2995a90a1f16
SPL ID: ba446257-56b6-616f-e053-2a95a90a1f16
Version: 1
Effective date: 2021-02-17
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 05:26:32

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA OSTEO	openfda.brand_name
generic name		ARNICA MONTANA ROOT - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - EQUISETUM HYEMALE - FUMARIC ACID - SUS SCROFA UMBILICAL CORD - SUS SCROFA OVARY - SUS SCROFA PLACENTA - COMFREY ROOT - SUCCINIC ACID - SILICON DIOXIDE -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-473-18	openfda.package_ndc
ndc	product	17089-473	openfda.product_ndc
ndc11	package	17089047318	derived:openfda.package_ndc
spl id		ba446257-56b6-616f-e053-2a95a90a1f16	id
spl set id		ba4462d6-9751-530f-e053-2995a90a1f16	set_id
unii		O3B55K4YKI	openfda.unii
unii		88XHZ13131	openfda.unii
unii		C8CV8867O8	openfda.unii
unii		97Z1WI3NDX	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		M9VVZ08EKQ	openfda.unii
unii		S7YTV04R8O	openfda.unii
unii		59677RXH25	openfda.unii
unii		118OYG6W3H	openfda.unii
unii		AB6MNQ6J6L	openfda.unii
unii		MUE8Y11327	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 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.