SILVAPLEX WOUND GEL- wound gel gel

SilvaPlex Wound Gel by

Drug Labeling and Warnings

SilvaPlex Wound Gel by is a Homeopathic medication manufactured, distributed, or labeled by AG Essence, AG Essence Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions: Clean area of dirt and debris. Apply a layer of Silva[lex Wound Gel Dressing to the affected area. If not covered apply 1 - 3 times daily or as needed. Between dressing changes maintain moist wound environment.

WARNINGS

Contact Veterinarian if pet has deep or puncture wounds or if symptoms persist or worsen after 5 days.

Store at room temperature and out of direct sunlight.

INACTIVE INGREDIENT

Inactive - Complez AG21 (Chelated Silver), Water, Polycationic Polymers, Glycerin, L-Arginine, Hemp CBD

INDICATIONS & USAGE

Indications for use: for relief of these symptoms due to minor Wounds,burns, Scrapes, Ulcerations or Minor Infections, Burning, Stinging, Itching, Redness, Minor Pain and Minor Inflammation.*

*These statements have not been evaluated by the FDA. This product is not intended to diagnose, treat cure or prevent any disease.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

For Animal Use Only

PURPOSE

Topical Antiseptic

ACTIVE INGREDIENT

Active - Argentum Metallicum (Metallic Silver) 10X, 20X, 30X HPUS

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SILVAPLEX WOUND GEL 
wound gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72363-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	5.9 g  in 118 g

Inactive Ingredients
Ingredient Name	Strength
POLYQUATERNIUM-4 (1600 MPA.S AT 2%) (UNII: YE8J8372VI)	8.85 g  in 118 g
ARGININE (UNII: 94ZLA3W45F)	2.36 g  in 118 g
WATER (UNII: 059QF0KO0R)	89.916 g  in 118 g
GLYCERIN (UNII: PDC6A3C0OX)	10.974 g  in 118 g

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72363-012-04	118 g in 1 JAR; Type 0: Not a Combination Product	03/24/2022	03/24/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/24/2022	03/24/2025

Labeler - AG Essence (068562165)

Registrant - AG Essence Inc. (068562165)

Establishment
Name	Address	ID/FEI	Business Operations
AG Essence		068562165	manufacture(72363-012)