ARGENTUM

Manufacturer
STANDARD HOMEOPATHIC COMPANY
Effective date
2021-10-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:31:40

Label at a glance#

ProductARGENTUM
Active ingredientSILVER NITRATE
Label structure9 sections

Dosage and administration

ADULTS: Dissolve 4 tablets under tongue 4 times a day. CHILDREN: Consult 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

OTC - DO NOT USE SECTION

Do not use if cap band is missing or broken.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - ASK DOCTOR 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.

Questions?

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 healthcare professional.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

INDICATIONS & USAGE SECTION

FATIGUE OR HEADACHE

OTC - PURPOSE SECTION

FATIGUE OR HEADACHE

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

ARGENTUM NIT. 6X

Principal Display Panel - 250 Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Standard

Homeopathic

Made in the USA Since 1903

NDC # 0360-0011-01

Homeopathic Medicine

ARGENTUM NIT.

6X

FATIGUE OR HEADACHE*

*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 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0360-00110360-0011-01

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
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
ACACIA5C5403N26OIACT
SILVER NITRATE95IT3W8JZEACTIB

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
cea7c137-795b-f07b-e053-2995a90a850e4a2880ab-d7ce-08f7-e054-00144ff8d46c2021-10-18WarningsExact identifier
spl id: cea7c137-795b-f07b-e053-2995a90a850e
spl set id: 4a2880ab-d7ce-08f7-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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