FDA.reportPublic FDA data

NDC 27426-016 - Keratex KCG

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
27426-016
Package NDCs from labels
27426-016-10
Manufacturer
Penleigh Irving Ltd
Effective date
2018-12-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Keratex KCG - Penleigh Irving LtdPenleigh Irving Ltd2018-12-21OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
27426-016-10KeratexKCG1 L in 1 BOTTLE, PLASTICLIQUID18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
27426-016KERATEX KCG (ALCOHOL AND WATER) LIQUID [PENLEIGH IRVING LTD]81 package rows20181222_4ca82b1d-ccd4-4326-b3da-30b45eeb471a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MKERATEX KCG (ALCOHOL AND WATER) LIQUID [PENLEIGH IRVING LTD]7
WaterACTIVE INGREDIENT059QF0KO0RKERATEX KCG (ALCOHOL AND WATER) LIQUID [PENLEIGH IRVING LTD]7
ALCOHOLACTIVE MOIETY3K9958V90MKERATEX KCG (ALCOHOL AND WATER) LIQUID [PENLEIGH IRVING LTD]7
WaterACTIVE MOIETY059QF0KO0RKERATEX KCG (ALCOHOL AND WATER) LIQUID [PENLEIGH IRVING LTD]7
LaponiteINACTIVE INGREDIENTD703131383KERATEX KCG (ALCOHOL AND WATER) LIQUID [PENLEIGH IRVING LTD]7

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 147 of 147 · 2,926 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Freeman Packaging Hand SanitizerALCOHOLJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.9827418a-3ab6-447b-8f8a-9eacb56d3a892017-10-09WarningsExact identifier
unii: 3K9958V90M
ONID WipeETHANOLONID Technology Corp83d8b8b6-6257-4553-9441-901bb02c3d602017-06-28Exact identifier
unii: 3K9958V90M
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
CVS Hand SanitizerALCOHOLCVSd0081c50-c0d2-436a-ba83-5d1982ae64b72015-08-17WarningsExact identifier
unii: 3K9958V90M
Instant Hand SanitizerALCOHOLSafetec of America, Inc.f9e30645-491b-4f54-acfd-f863ee2356072013-08-07WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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