Plantain Spruce Cough

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: Plantain Spruce Cough
Generic name: PLANTAIN SPRUCE COUGH
Manufacturer: Uriel Pharmacy Inc.
Product type: HUMAN OTC DRUG
SPL set ID: d6a99616-4a08-0909-e053-2995a90a0d2f
SPL ID: 2b2402e5-9d9b-a55e-e063-6394a90a6214
Version: 6
Effective date: 2025-01-07
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:56:01

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		Plantain Spruce Cough	openfda.brand_name
generic name		PLANTAIN SPRUCE COUGH	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc.	openfda.manufacturer_name
ndc	package	48951-8390-1	openfda.package_ndc
ndc	product	48951-8390	openfda.product_ndc
ndc11	package	48951839001	derived:openfda.package_ndc
spl id		2b2402e5-9d9b-a55e-e063-6394a90a6214	id
spl set id		d6a99616-4a08-0909-e053-2995a90a0d2f	set_id
unii		QR44N9XPJQ	openfda.unii
unii		LZB7TFX1LT	openfda.unii
unii		D77PG8S4KK	openfda.unii
unii		608DGJ6815	openfda.unii
unii		S003A158SB	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		62I3C8233L	openfda.unii
unii		TJ55Y9N2M4	openfda.unii
unii		3BN57UN4US	openfda.unii
unii		97S2809V5R	openfda.unii
unii		QNS6W5US1Z	openfda.unii
unii		3MLB4858X7	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. Do not use if safety seal is broken or missing. SHAKE WELL BEFORE USE. REFRIGERATE AFTER OPENING. BEST WHEN USED WITHIN 30 DAYS OF OPENING.

Reported adverse events (FAERS/openFDA)#

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