FDA.reportPublic FDA data

NDC 0813-0012 - Ferretts

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
0813-0012
Package NDCs from labels
0813-0012-06
Manufacturer
Pharmics, Inc.
Effective date
2015-01-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ferretts Iron SupplementPharmics, Inc.2015-01-08DIETARY SUPPLEMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0813-0012-06Ferretts60 in 1 BOTTLETABLET, FILM COATED601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0813-0012FERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]11 package rows20150113_10ae0336-a368-4597-8a21-35afc12ba124.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0813-0012-06EA - Each0813-00123f5cef08-21b0-4b19-93f3-adbf67d734d712015-02-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Ferrous FumarateACTIVE INGREDIENTR5L488RY0QFERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]1
FERROUS CATIONACTIVE MOIETYGW89581OWRFERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]1
Cellulose, MicrocrystallineINACTIVE INGREDIENTOP1R32D61UFERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48FERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]1
EthylcellulosesINACTIVE INGREDIENT7Z8S9VYZ4BFERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]1
Magnesium StearateINACTIVE INGREDIENT70097M6I30FERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]1
Silicon DioxideINACTIVE INGREDIENTETJ7Z6XBU4FERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]1
Stearic AcidINACTIVE INGREDIENT4ELV7Z65APFERRETTS (FERROUS FUMARATE) TABLET, FILM COATED [PHARMICS, INC.]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 32 of 32 · 624 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ReHydrationADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS (BOVINE), KALI PHOSPHORICUM, NATRUM MURIATICUM, SARSAPARILLA, SILICEA, TARAXACUM OFFICINALE, THYROIDINUM (BOVINE)Energetix Corp9883c502-9782-451e-9eec-c54d7b054f312017-01-31WarningsExact identifier
unii: ETJ7Z6XBU4
Tox-ChordALFALFA, ALUMINA, BENZOICUM ACIDUM, CARBONEUM, CETRARIA ISLANDICA, FOLLICULINUM, FUCUS VESICULOSUS, FUMARICUM ACIDUM, HEPAR SUIS, KALI CARBONICUM, KREOSOTUM, NATRUM MURIATICUM, PARAFFINUM, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PIX LIQUIDA, PLANTAGO MAJOR, PLUMBUM METALLICUM, PULSATILLA (VULGARIS), RADIUM BROMATUM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM OFFICINALE, TABACUM, TEREBINTHINA, THYROIDINUM (BOVINE), TRITICUM REPENS, ZINCUM OXYDATUMEnergetix Corp6b0d1628-b20d-426e-9c84-5cceadca3f452016-11-11WarningsExact identifier
unii: ETJ7Z6XBU4
ThyrotoxCHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEABioActive Nutritional, Inc.e229a260-13f3-4136-b325-9a8954f8a3272016-08-10WarningsExact identifier
unii: ETJ7Z6XBU4
TeethingARNICA MONTANA, TRIFOLIUM PRATENSE, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CHAMOMILLA, KREOSOTUM, SILICEABioActive Nutritional, Inc.f39c9feb-f567-43a2-a026-2a581aeeed9d2016-07-27WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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