Betonica Rosmarinus

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: Betonica Rosmarinus
Generic name: BETONICA ROSMARINUS
Manufacturer: Uriel Pharmacy Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 329763c8-92aa-4c61-9599-9ae183db239e
SPL ID: 2c524d29-133e-1adc-e063-6294a90a305a
Version: 4
Effective date: 2025-01-22
Source export date: 2026-11-06
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2cac198adf50bf0f7077ca012f418bbee1fb171f907f83d6a83048d9770d345b/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:11:35

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Betonica Rosmarinus	openfda.brand_name
generic name		BETONICA ROSMARINUS	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc.	openfda.manufacturer_name
ndc	package	48951-2062-1	openfda.package_ndc
ndc	product	48951-2062	openfda.product_ndc
ndc11	package	48951206201	derived:openfda.package_ndc
spl id		2c524d29-133e-1adc-e063-6294a90a305a	id
spl set id		329763c8-92aa-4c61-9599-9ae183db239e	set_id
unii		8JM482TI79	openfda.unii
unii		UO9989Y17N	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: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

Reported adverse events (FAERS/openFDA)#

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