NDC 69420-8004 - ZENPHOR WOUND

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 69420-8004
Package NDCs from labels: 69420-8004-1
Manufacturer: SA3, LLC
Effective date: 2021-08-26
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ZENPHOR WOUND - SA3, LLC	SA3, LLC	2021-08-26	MEDICAL DEVICE

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69420-8004-1	GM - Gram	69420-8004	873274fb-565e-4d42-8cfe-2d1fb60c34dd	1	2022-03-09

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 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lidocaine 4 Percent	LIDOCAINE	SA3, LLC	651710db-3c50-4bcf-b7cc-9ed24f663427	2024-12-09	Warnings	Name fallback manufacturer name: SA3, LLC
Capsaicin	CAPSAICIN	SA3, LLC	5617e91d-e650-4a0d-8565-b8288ea41c77	2024-12-09	Warnings	Name fallback manufacturer name: SA3, LLC
Capsaicin	CAPSAICIN	SA3, LLC	7950aabc-4724-4add-a96e-62ab7e75d4fc	2024-12-09	Warnings	Name fallback manufacturer name: SA3, LLC
Naproxen Sodium	NAPROXEN SODIUM	SA3, LLC	313dd447-4b9f-4e5b-8ca9-4a2a5a1a53d9	2019-04-23	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: SA3, LLC

Reported adverse events (FAERS/openFDA)#

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