NDC 69573-888-11 - Chitoprex 101

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: 69573-888
Requested NDC: 69573-888-11
Package NDCs from labels: 69573-888-11, 69573-888-33
Manufacturer: 38 Biotech Laboratory LLC
Effective date: 2015-02-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Chitoprex 101 - 38 Biotech Laboratory LLC	38 Biotech Laboratory LLC	2015-02-27	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69573-888-33	2020-01-31	C162847	48780-1	9d75b9d0-9eaa-f424-e053-dadaa90a57ce	Chitoprex

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69573-888-11	Chitoprex101	500 mg in 1 CAPSULE	CAPSULE	500		1
69573-888-33	Chitoprex101	30 in 1 BOTTLE	CAPSULE	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69573-888	CHITOPREX 101 (38 BIOTECH LABORATORY LLC) CAPSULE [38 BIOTECH LABORATORY LLC]	1	Legacy NDC, 2 package rows	20150618_10162a50-f00a-4426-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CHITOSAN OLIGOSACCHARIDE	ACTIVE INGREDIENT	23R93M6Y64	CHITOPREX 101 (38 BIOTECH LABORATORY LLC) CAPSULE [38 BIOTECH LABORATORY LLC]	1
CHITOSAN OLIGOSACCHARIDE	ACTIVE MOIETY	23R93M6Y64	CHITOPREX 101 (38 BIOTECH LABORATORY LLC) CAPSULE [38 BIOTECH LABORATORY LLC]	1
Nori	INACTIVE INGREDIENT	477TV3P5UX	CHITOPREX 101 (38 BIOTECH LABORATORY LLC) CAPSULE [38 BIOTECH LABORATORY LLC]	1

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bispit Canada Ltd.	BISPIT LIVER RESTORATION TABLETS	Bispit Canada Ltd.	36e35682-57cb-f60f-e063-6394a90aafa5	2025-06-06	Warnings	Exact identifier unii: 23R93M6Y64
10162a50-f00b-4426-e054-00144ff88e88			10162a50-f00a-4426-e054-00144ff88e88	2015-02-27	Warnings	Exact identifier spl id: 10162a50-f00b-4426-e054-00144ff88e88 spl set id: 10162a50-f00a-4426-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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