SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE

Manufacturer: Natural Immunogenics Corp.dba SOVEREIGN NATURALS
Effective date: 2025-11-24
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 02:35:26

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 description

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0684088500074	GTIN-13: 0684088500074 EAN-13: 0684088500074 GTIN-12: 684088500074 UPC-A: 684088500074 GTIN storage (14 digits): 00684088500074	updatedlabel1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
52166-018-01	SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE	14.5 mL in 1 TUBE	GEL	14.5	5
52166-018-01	SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE	1 in 1 CARTON	GEL	1	5
52166-018-02	SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE	1 in 1 CARTON	GEL	1	5
52166-018-02	SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE	29 mL in 1 TUBE	GEL	29	5

Products#

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

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

SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE
Argentum Metallicum
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)
SODIUM HYDROXIDE
SILVER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52166-018	52166-018-01, 52166-018-02

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)	HHT01ZNK31	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
SILVER	3M4G523W1G	ACTIB

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
SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE	ARGENTUM METALLICUM	Natural Immunogenics Corp.dba SOVEREIGN NATURALS	bfb30395-e9a7-4d9e-b2f3-74f4710bbefa	2025-11-24	Warnings	Exact identifier ndc (package): 52166-018-01 ndc (package): 52166-018-02 ndc (product): 52166-018 ndc11 (package): 52166001801 ndc11 (package): 52166001802 spl id: 445759d0-4d7f-aeee-e063-6394a90ae838 spl set id: bfb30395-e9a7-4d9e-b2f3-74f4710bbefa

Reported adverse events (FAERS/openFDA)#

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