Banda-Sil Liquid Gel

Manufacturer
AG Essence Inc
Effective date
2024-04-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:26:41

Label at a glance#

ProductBanda-Sil Liquid Gel
Active ingredientSILVER
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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 SECTION

Inactive Ingredients:

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

INDICATIONS & USAGE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings:

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

OTC - PURPOSE SECTION

Topical Antiseptic

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

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

Banda-Sil Spray Gel Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Banda-Sil Spray Gel BoxBanda-Sil Spray Gel Box

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72363-005-03Banda-Sil Liquid Gel28.5 g in 1 BOTTLE, SPRAYGEL28.54
72363-005-03Banda-Sil Liquid Gel1 in 1 BOXGEL14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72363-005BANDA-SIL LIQUID GEL (ARGENTUM METALLICUM) GEL [AG ESSENCE INC]4Legacy NDC, 2 package rows20240420_c445ba28-5a66-6dc4-e053-2a95a90afe6d.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72363-00572363-005-03

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
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SILVER3M4G523W1GACTIB
ARGININE94ZLA3W45FIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1672ca82-b754-8bbf-e063-6294a90a1d52c445ba28-5a66-6dc4-e053-2a95a90afe6d2024-04-19WarningsExact identifier
spl id: 1672ca82-b754-8bbf-e063-6294a90a1d52
spl set id: c445ba28-5a66-6dc4-e053-2a95a90afe6d

Reported adverse events (FAERS/openFDA)#

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