Home NDC 72363-018 PetSilver Wound 8
Product NDC 72363-018
11-digit product format 723630018
Labeler code 72363
Product ID 72363-018_45eec4d5-1e70-49d3-e063-6294a90a1727
Type HUMAN OTC DRUG
Nonproprietary name Argentum Metallicum
Dosage form SPRAY
Route TOPICAL
Labeler AG Essence
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance SILVER
Active strength .007 g/237g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base PetSilver Wound 8
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILVER .007 g/237g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3M4G523W1G Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72363-018-01 PetSilver Wound 8 237 g in 1 BOTTLE SPRAY 237 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72363-018 PETSILVER WOUND 8 (ARGENTUM METALLICUM) SPRAY [AG ESSENCE] 2 Current NDC, 1 package rows 20250112_0c79d23d-ab11-a626-e063-6394a90afeb5.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72363-018-01 72363001801 237 g in 1 BOTTLE (72363-018-01) 237 g 2024-01-01 No No Current