NDC 37662-2275-01 - Scutellaria Lateriflora

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
37662-2275
Requested NDC
37662-2275-01
Package NDCs from labels
37662-2275-1, 37662-2275-2, 37662-2275-3, 37662-2275-4, 37662-2275-01
Manufacturer
Hahnemann Laboratories, INC.
Effective date
2023-01-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Scutellaria Lateriflora - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-01-09HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2275-1Scutellaria Lateriflora200 in 1 VIAL, GLASSPELLET2001
37662-2275-2Scutellaria Lateriflora500 in 1 VIAL, GLASSPELLET5001
37662-2275-3Scutellaria Lateriflora3000 in 1 BOTTLE, GLASSPELLET30001
37662-2275-4Scutellaria Lateriflora10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2275SCUTELLARIA LATERIFLORA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 4 package rows20230111_f1dd6d9b-f1d7-0820-e053-2a95a90a82a6.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 6 of 6 · 101 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
StressARALIA QUIN, PASSIFLORA, SCUTELLARIA, VALERIANA, ARSENICUM ALB, AUR MET, CALC CARB, COFFEA CRUDA, IGNATIA, KALI PHOS, LYCOPUS, PHOSPHORUS, STAPHYSAGRIAZorex Internationald0527396-7b7f-4252-be0f-d3aa74c25e0e2018-12-21WarningsExact identifier
unii: 7BP4DH5PDC

Reported adverse events (FAERS/openFDA)#

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