BANDA-SIL LIQUID GEL- argentum metallicum gel

Banda-Sil Liquid Gel by

Drug Labeling and Warnings

Banda-Sil Liquid Gel by is a Homeopathic medication manufactured, distributed, or labeled by AG Essence Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions For Use:

Clear wound area of dirt and debris.

Spray the affected area with Banda-Sil Silver Liquid Gel Spray and allow to dry.

Cover with a sterile gauze or appropriate secondary dressing and secure in place.

Reapply 1-3 times daily or as needed.

Between dressing changes maintain a moist wound environment.

WARNINGS

Warnings:

For External Use Only. Keep out of reach of children.

Consult a doctor if condition worsens or does not improve in seven (7) days. Ask a doctor before use if you have deep or puncture wounds, serious bleeding, or servious burns.

INACTIVE INGREDIENT

Inactive Ingredients:

Complex AG21, Water, Polycationic Polymers, Glycerin, L-Arginine

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, minor inflammation.

KEEP OUT OF REACH OF CHILDREN

Warnings:

For External Use Only. Keep out of reach of children.

PURPOSE

Topical Antiseptic

ACTIVE INGREDIENT

Active Ingredient

Argentum Metallicum (Metallic Silver 10X 20X 30X HPUS)

Banda-Sil Spray Gel Box

INGREDIENTS AND APPEARANCE

BANDA-SIL LIQUID GEL 
argentum metallicum gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72363-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	1 g  in 28.5 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	27.13 g  in 28.5 g
GLYCERIN (UNII: PDC6A3C0OX)	0.285 g  in 28.5 g
ARGININE (UNII: 94ZLA3W45F)	0.085 g  in 28.5 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72363-005-03	1 in 1 BOX	06/25/2021
1		28.5 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/25/2021

Labeler - AG Essence Inc (068562165)

Establishment
Name	Address	ID/FEI	Business Operations
AG Essence Inc		068562165	manufacture(72363-005)