FDA.reportPublic FDA data

PLUMBUM

Manufacturer
STANDARD HOMEOPATHIC COMPANY
Effective date
2021-12-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:24:34

Label at a glance#

ProductPLUMBUM
Active ingredientLEAD
Label structure8 sections

Dosage and administration

Adults: Dissolve 4 tablets under tongue 4 times a day. Children: Consult a healthcare professional

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Made according to the Homeopathic Pharmacopoeia of the United States since 1903.

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

Do not use if cap band is missing or broken.

SPL UNCLASSIFIED SECTION

If you are pregnant or nursing, consult a licensed health care professional before using this product.

SPL UNCLASSIFIED SECTION

If symptoms persist for 7 days or worsen, contact a licensed practitioner.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of the reach of children.

SPL UNCLASSIFIED SECTION

To be used according to label indications and/or standard homeopathic indications.

OTC - QUESTIONS SECTION

Standard Homeopathic Company

Los Angeles, CA 90061

Questions? 800-624-9659

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 4 tablets under tongue 4 times a day.

Children: Consult a healthcare professional

INACTIVE INGREDIENT SECTION

In a base of Acacia Gum and Lactose N.F.

OTC - ACTIVE INGREDIENT SECTION

PLUMBUM 6X

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

CONSTIPATION OR CRAMPS

Principal Display Panel -- 250 Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Standard

Homeopathic
Made in the USA Since 1903

NDC # 0360-0310-01

Homeopathic Medicine

PLUMBUM

6X

CONSTIPATION OR CRAMPS*

*Claims based on traditional homeopathic practice,

not accepted medical evidence. Not FDA evaluated.

250 TABLETS

labellabel

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0360-03100360-0310-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACACIA5C5403N26OIACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
LEAD2P299V784PACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d27f27fe-7713-a220-e053-2995a90af29f4db01075-e266-48cd-e054-00144ff8d46c2021-12-06WarningsExact identifier
spl id: d27f27fe-7713-a220-e053-2995a90af29f
spl set id: 4db01075-e266-48cd-e054-00144ff8d46c