SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE- argentum metallicum gel

SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE by

Drug Labeling and Warnings

SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE by is a Homeopathic medication manufactured, distributed, or labeled by Natural Immunogenics Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ingredients

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

PURPOSE

Purpose

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

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WARNINGS

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

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

CARBOPOL, SILVER HYDROSOL AND SODIUM HYDROXIDE

Product label

INGREDIENTS AND APPEARANCE

SOVEREIGN SILVER FIRST AID HOMEOPATHIC MEDICINE 
argentum metallicum gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52166-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	30 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52166-018-01	1 in 1 CARTON	08/25/2024
1		14.5 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 52166-018-02	1 in 1 CARTON	08/25/2024
2		29 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/25/2024

Labeler - Natural Immunogenics Corp. (048744085)

Registrant - Natural Immunogenics Corp. (048744085)

Establishment
Name	Address	ID/FEI	Business Operations
Natural Immunogenics Corp.		048744085	manufacture(52166-018)