Argentum Metallicum - Natural Immunogenics Corp.dba SOVEREIGN NATURALS

Manufacturer
Natural Immunogenics Corp.dba SOVEREIGN NATURALS
Effective date
2026-10-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-10-15 01:01:36

Label at a glance#

ProductSOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE
Active ingredientSILVER
Label structure8 sections

Indications and uses

FIRST AID GEL TO HELP PREVENT INFECTION IN MINOR CUTS, SCRAPES, BURNS, SKIN ERUPTIONS FROM ECZEMA, RASHES, BLISTERS, SUNBURN, RAZOR BURN, MINOR NICKS, REDNESS AND MINOR INFLAMMATION

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ingredients

ACTIVE:  ARGENTUM METALLICUM 10X, 20X, 30X HPUS

OTC - PURPOSE SECTION

Purpose

TOPICAL HEALING – COMBATS AND QUICKLY HEALS MINOR SKIN INFECTIONS, WOUNDS AND BURNS

Uses

INDICATIONS & USAGE SECTION

FIRST AID GEL TO HELP PREVENT INFECTION IN MINOR CUTS, SCRAPES, BURNS, SKIN ERUPTIONS FROM ECZEMA, RASHES, BLISTERS, SUNBURN, RAZOR BURN, MINOR NICKS, REDNESS AND MINOR INFLAMMATION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

Warnings

FOR EXTERNAL USE ONLY.ASK A DOCTOR BEFORE USE IF YOU HAVE DEEP OR PUNCTURE WOUNDS, ANIMAL BITES OR SERIOUS BURNS. KEEP OUT OF REACH OF CHILDREN. STOP AND ASK A DOCTOR IF SYMPTOMS PERSIST OR WORSEN AFTER 3 DAYS OF USE. DO NOT USE IF THE SEAL IS BROKEN.

DOSAGE & ADMINISTRATION SECTION

Directions

CLEAN AFFECTED AREA. APPLY A LIBERAL CONSISTENT LAYER OF FIRST AID GEL OVER AFFECTED AREA. LEAVE WET OR BANDAGE FOR OPTIMAL RESULTS. REPEAT 3 TIMES PER DAY OR AS OFTEN AS NEEDED TO RELIEVE SYMPTOMS. SAFE ON SENSITIVE SKIN.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

CARBOPOL, SILVER HYDROSOL AND SODIUM HYDROXIDE

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130684088500074GTIN-13: 0684088500074
EAN-13: 0684088500074
GTIN-12: 684088500074
UPC-A: 684088500074
GTIN storage (14 digits): 00684088500074
updatedlabel1.jpg

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
52166-01852166-018-01, 52166-018-02

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-11-24full-release2026-06-01 02:35:26

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
445759d0-4d7f-aeee-e063-6394a90ae838bfb30395-e9a7-4d9e-b2f3-74f4710bbefa2025-11-24WarningsExact identifier
spl set id: bfb30395-e9a7-4d9e-b2f3-74f4710bbefa

Reported adverse events (FAERS/openFDA)#

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