Plantago Primula

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: Plantago Primula
Generic name: PLANTAGO PRIMULA
Manufacturer: Uriel Pharmacy Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 25545753-2d00-47fe-b318-b7e4a47c3d0d
SPL ID: 2c522c57-994b-4e02-e063-6394a90a1f12
Version: 4
Effective date: 2025-01-22
Source export date: 2026-09-28
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/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:20

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Plantago Primula	openfda.brand_name
generic name		PLANTAGO PRIMULA	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc.	openfda.manufacturer_name
ndc	package	48951-8034-1	openfda.package_ndc
ndc	product	48951-8034	openfda.product_ndc
ndc11	package	48951803401	derived:openfda.package_ndc
spl id		2c522c57-994b-4e02-e063-6394a90a1f12	id
spl set id		25545753-2d00-47fe-b318-b7e4a47c3d0d	set_id
unii		7DC28K241X	openfda.unii
unii		W5BET37294	openfda.unii
unii		32IT7G8BAW	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.