NDC 37662-0891-01 - Kali Nitricum

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: 37662-0891
Requested NDC: 37662-0891-01
Package NDCs from labels: 37662-0891-1, 37662-0891-2, 37662-0891-3, 37662-0891-01
Manufacturer: Hahnemann Laboratories, INC.
Effective date: 2022-07-14
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Kali Nitricum - Hahnemann Laboratories, INC.	Hahnemann Laboratories, INC.	2022-07-14	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
37662-0891-1	Kali Nitricum	200 in 1 VIAL, GLASS	PELLET	200	1
37662-0891-2	Kali Nitricum	1200 in 1 BOTTLE, GLASS	PELLET	1200	1
37662-0891-3	Kali Nitricum	4000 in 1 BOTTLE, GLASS	PELLET	4000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37662-0891	KALI NITRICUM PELLET [HAHNEMANN LABORATORIES, INC.]	1	Current NDC, Legacy NDC, 3 package rows	20220716_e3cada58-aa1a-8792-e053-2a95a90a388f.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 11 of 11 · 201 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ionite H	SODIUM FLUORIDE, POTASSIUM NITRATE	Dharma Research, Inc.	642fec99-c5c5-4ef2-986e-5b5f7cf460de	2015-08-02	Warnings, Adverse reactions	Exact identifier unii: RU45X2JN0Z

Reported adverse events (FAERS/openFDA)#

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