NDC 86112-1821 - Facil 1.1 Concentrate

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
86112-1821
Package NDCs from labels
86112-1821-1, 86112-1821-2, 86112-1821-3, 86112-1821-4
Manufacturer
Dairy Alarm LLC | Thatcher Company of New York
Effective date
2019-11-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Facil 1.1 Concentrate - Dairy Alarm LLC | Thatcher Company of New YorkDairy Alarm LLC | Thatcher Company of New York2019-11-06OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86112-1821-1Facil 1.1 Concentrate2 kg in 1 PAILLIQUID22
86112-1821-2Facil 1.1 Concentrate7 kg in 1 PAILLIQUID72
86112-1821-3Facil 1.1 Concentrate27 kg in 1 DRUMLIQUID272
86112-1821-4Facil 1.1 Concentrate135 kg in 1 TANKLIQUID1352

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86112-1821FACIL 1.1 CONCENTRATE (NONE) LIQUID [DAIRY ALARM LLC]24 package rows20191107_23980830-62fe-4e0a-8908-cc6fa79fc628.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
Glucose Control T015SYZYGIUM JAMBOLANUM, GLANDULA SUPRARENALIS SUIS, HYDRASTIS CANADENSIS, HYPOPHYSIS SUIS, PANCREAS SUIS, PHASEOLUS, ACETICUM ACIDUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, URANIUM NITRICUMGuangzhou Renuma Medical Systems Co., Ltd3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b2017-10-26WarningsExact identifier
unii: 33X04XA5AT

Reported adverse events (FAERS/openFDA)#

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