NDC 37662-1906-01 - Paeonia Officinalis

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
37662-1906
Requested NDC
37662-1906-01
Package NDCs from labels
37662-1906-1, 37662-1906-2, 37662-1906-3, 37662-1906-4, 37662-1906-01
Manufacturer
Hahnemann Laboratories, INC.
Effective date
2022-11-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Paeonia Officinalis - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2022-11-09HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-1906-1Paeonia Officinalis80 in 1 VIAL, GLASSPELLET801
37662-1906-2Paeonia Officinalis200 in 1 VIAL, GLASSPELLET2001
37662-1906-3Paeonia Officinalis1200 in 1 BOTTLE, GLASSPELLET12001
37662-1906-4Paeonia Officinalis4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-1906PAEONIA OFFICINALIS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 4 package rows20221115_ed03a980-af17-59d4-e053-2995a90a583e.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 5 of 5 · 81 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hemorrhoid GelACHILLEA MILLEFOLIUM, AESCULUS HIPPOCASTANUM, HAMAMELIS VIRGINIANA, RUSCUS ACULEATUS, ALOE SOCOTRINA, PAEONIA OFFICINALIS, IGNATIA AMARA, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORUS, PODOPHYLLUM PEITATUM, PULSATILLA, RATANHIA, CHELIDONIUM MAJUS, SULPHURNatural Creations, Incd2016513-9b47-490d-9396-766db4cafecd2018-12-21WarningsExact identifier
unii: 8R564U2E1P

Reported adverse events (FAERS/openFDA)#

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