PLUMBUM METALLICUM

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: PLUMBUM METALLICUM
Generic name: PLUMBUM METALLICUM
Manufacturer: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Product type: HUMAN OTC DRUG
SPL set ID: de421f83-606f-4581-8180-9fd4ee8dc76f
SPL ID: cd13512b-ebdb-a3ed-e053-2a95a90a9d27
Version: 4
Effective date: 2021-09-28
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:56:54

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		PLUMBUM METALLICUM	openfda.brand_name
generic name		PLUMBUM METALLICUM	openfda.generic_name
manufacturer name		Rxhomeo Private Limited d.b.a. Rxhomeo, Inc	openfda.manufacturer_name
ndc	package	15631-0353-0	openfda.package_ndc
ndc	package	15631-0353-3	openfda.package_ndc
ndc	package	15631-0353-4	openfda.package_ndc
ndc	package	15631-0353-1	openfda.package_ndc
ndc	package	15631-0353-6	openfda.package_ndc
ndc	package	15631-0353-7	openfda.package_ndc
ndc	package	15631-0353-5	openfda.package_ndc
ndc	package	15631-0353-2	openfda.package_ndc
ndc	product	15631-0353	openfda.product_ndc
ndc11	package	15631035300	derived:openfda.package_ndc
ndc11	package	15631035301	derived:openfda.package_ndc
ndc11	package	15631035305	derived:openfda.package_ndc
ndc11	package	15631035302	derived:openfda.package_ndc
ndc11	package	15631035304	derived:openfda.package_ndc
ndc11	package	15631035307	derived:openfda.package_ndc
ndc11	package	15631035306	derived:openfda.package_ndc
ndc11	package	15631035303	derived:openfda.package_ndc
spl id		cd13512b-ebdb-a3ed-e053-2a95a90a9d27	id
spl set id		de421f83-606f-4581-8180-9fd4ee8dc76f	set_id
unii		2P299V784P	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 This product is to be used for self-limiting conditions If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product Keep this and all medication out of reach of children

Reported adverse events (FAERS/openFDA)#

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