Plumbum 8X

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2019-12-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:11:37

Label at a glance#

ProductPlumbum 8X

Active ingredientLEAD

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

DOSAGE & ADMINISTRATION SECTION

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Plumbum (Lead) 8X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt, Lactose

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains traces of lactose. 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.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Plumbum 8X Ampules

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-8362-1	2025-01-30	C162847	48780-1	2cef2736-a762-d83d-e063-dadaa90ab31f	Plumbum 8X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8362-1	Plumbum 8X	10 in 1 BOX	LIQUID	10		1
48951-8362-1	Plumbum 8X	1 mL in 1 AMPULE	LIQUID	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8362	PLUMBUM 8X LIQUID [URIEL PHARMACY INC.]	1	Legacy NDC, 2 package rows	20191210_994b027a-d7d2-7fb1-e053-2a95a90a3f96.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

Plumbum 8X
LEAD
SODIUM CHLORIDE
LACTOSE, UNSPECIFIED FORM
ANHYDROUS LACTOSE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-8362	48951-8362-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LEAD	2P299V784P	ACTIB
SODIUM CHLORIDE	451W47IQ8X	IACT
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
994b027a-d7d3-7fb1-e053-2a95a90a3f96			994b027a-d7d2-7fb1-e053-2a95a90a3f96	2019-12-09	Warnings	Exact identifier spl id: 994b027a-d7d3-7fb1-e053-2a95a90a3f96 spl set id: 994b027a-d7d2-7fb1-e053-2a95a90a3f96

Reported adverse events (FAERS/openFDA)#

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