Banda-Sil Liquid Gel

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	72363-005		I	Inactivated by FDA		2026-10-05
excluded package	package	72363-005	72363-005-03	I	Inactivated by FDA		2026-10-05

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

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
1681bc73-b05f-12c3-1075-382ae39f449c	Product name	1	20140508

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72363-005-03	Banda-Sil Liquid Gel	28.5 g in 1 BOTTLE, SPRAY	GEL	28.5		4
72363-005-03	Banda-Sil Liquid Gel	1 in 1 BOX	GEL	1		4

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72363-005	BANDA-SIL LIQUID GEL (ARGENTUM METALLICUM) GEL [AG ESSENCE INC]	4	Legacy NDC, 2 package rows	20240420_c445ba28-5a66-6dc4-e053-2a95a90afe6d.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3M4G523W1G	SILVER	7440-22-4	SILVER

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
72363-005-03	72363000503	1 BOTTLE, SPRAY in 1 BOX (72363-005-03) > 28.5 g in 1 BOTTLE, SPRAY	2021-06-25	2023-11-30	No	No	Current