NDC 70434-103-01 - EDP BROWN

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: 70434-103
Requested NDC: 70434-103-01
Package NDCs from labels: 70434-103-01, 70434-103-02
Manufacturer: EDP Inc. | Kirpal Export Overseas
Effective date: 2019-01-15
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
EDP BROWN - EDP Inc. \| Kirpal Export Overseas	EDP Inc. \| Kirpal Export Overseas	2019-01-15	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70434-103-02	2021-01-29	C162847	48780-1	ba0f9c33-2440-a910-e053-dadaa90a0b85	EDP BROWN

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70434-103-01	EDP BROWN	100 g in 1 BAG	POWDER	100		4
70434-103-02	EDP BROWN	1 in 1 PACKAGE	POWDER	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70434-103	EDP BROWN (INDIGOFERA TINCTORIA LEAF) POWDER [EDP INC.]	4	Legacy NDC, 2 package rows	20190116_42c4e982-94cf-4882-bdce-ef951d367a05.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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
7f899eae-76eb-a1e8-e053-2991aa0a0c09			42c4e982-94cf-4882-bdce-ef951d367a05	2019-01-15	Warnings	Exact identifier spl id: 7f899eae-76eb-a1e8-e053-2991aa0a0c09 spl set id: 42c4e982-94cf-4882-bdce-ef951d367a05

Reported adverse events (FAERS/openFDA)#

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