SOVEREIGN SILVER- argentum metallicum gel

Sovereign Silver by

Drug Labeling and Warnings

Sovereign Silver 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 and 30x HPUS

INACTIVE INGREDIENT

INACTIVE: Silver hydrosol,

carbopol and sodium hydroxide

PURPOSE

Purpose

First Aid Gel

Homeopathic medicine

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Adult supervision required

WARNINGS

Warnings. For external

use only. Ask a doctor before use if

you have deep or puncture wounds, animal bites or serious burns.

ASK DOCTOR

Stop and ask a doctor if

symptoms persist or worsen after 3 days of use. Do not use if

seal is broken

DOSAGE & ADMINISTRATION

Enter section text here Directions. Clean affected area.

Apply a liberal, consistent layer of First Aid Gel. Leave wet or bandage for

optimal results. Repeat 3 times per day or as often as needed to relieve symptoms.

For sensitive skin.

INDICATIONS & USAGE

Indications for Use: For relief of these symptoms due to

minor wounds and burns, bruises, ulcerations, sunburn, razor burns,

scrapes, rashes, blisters, bug bites and skin eruptions from acne, eczema

or minor infection:

burning

stinging

itching

redness

stiffness

minor pain

minor inflammation

52166-002-01

52166-002-02

INGREDIENTS AND APPEARANCE

SOVEREIGN SILVER  
argentum metallicum gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52166-002
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 TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52166-002-01	1 in 1 BOX	01/01/2009
1		29 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 52166-002-02	1 in 1 BOX	01/01/2009
2		59 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/01/2009

Labeler - Natural Immunogenics Corp. (048744085)

Registrant - Natural Immunogenics Corp. (048744085)

Establishment
Name	Address	ID/FEI	Business Operations
Natural Immunogenics Corp.		048744085	manufacture(52166-002)