Plantago Pyrite

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 Pyrite
Generic name: PLANTAGO PYRITE
Manufacturer: Uriel Pharmacy Inc.
Product type: HUMAN OTC DRUG
SPL set ID: ce4ca5f0-1760-400a-b9bb-6efa3420ba19
SPL ID: 3eeff4b6-1ca0-fc7c-e063-6394a90a15b9
Version: 5
Effective date: 2025-09-16
Source export date: 2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:39:27

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		Plantago Pyrite	openfda.brand_name
generic name		PLANTAGO PYRITE	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc.	openfda.manufacturer_name
ndc	package	48951-8036-1	openfda.package_ndc
ndc	product	48951-8036	openfda.product_ndc
ndc11	package	48951803601	derived:openfda.package_ndc
spl id		3eeff4b6-1ca0-fc7c-e063-6394a90a15b9	id
spl set id		ce4ca5f0-1760-400a-b9bb-6efa3420ba19	set_id
unii		7DC28K241X	openfda.unii
unii		MN18OTN73W	openfda.unii
unii		91GQH8I5F7	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		065C5D077J	openfda.unii
unii		343455G79K	openfda.unii
unii		2I1RTO1MBR	openfda.unii
unii		1W0775VX6E	openfda.unii
unii		CE3G3J56LR	openfda.unii
unii		132N09W4PR	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. Contains traces of lactose. 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.