SilvaPlex Wound

Product NDC
72363-015
11-digit product format
723630015
Labeler code
72363
Product ID
72363-015_2b48d0a7-b8dc-21ae-e063-6294a90a9ebc
Type
HUMAN OTC DRUG
Nonproprietary name
Argentum Metallicum
Dosage form
SPRAY
Route
TOPICAL
Labeler
AG Essence
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-12-06
Substance
SILVER
Active strength
.047 g/236g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SilvaPlex Wound
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILVER.047 g/236g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3M4G523W1GInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0a483bdc-f8de-c2db-e063-6394a90ad373Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
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
72363-015-01SilvaPlex Wound236 g in 1 BOTTLESPRAY2362

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72363-015SILVAPLEX WOUND (ARGENTUM METALLICUM) SPRAY [AG ESSENCE]2Current NDC, 1 package rows20250112_0a483bdc-f8de-c2db-e063-6394a90ad373.zip

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
SilvaPlex WoundARGENTUM METALLICUMAG Essence0a483bdc-f8de-c2db-e063-6394a90ad3732025-01-09WarningsExact identifier
ndc (product): 72363-015

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72363-015-0172363001501236 g in 1 BOTTLE (72363-015-01) 236 g2023-12-06NoNoCurrent