NDC 53439-100-01 - Cut Care Alcohol Prep Pad

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
53439-100
Requested NDC
53439-100-01
Package NDCs from labels
53439-100-01, 53439-100-10
Manufacturer
Zeus Medical Holdings LLC
Effective date
2013-09-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cut Care Alcohol Prep Pad - Zeus Medical Holdings LLCZeus Medical Holdings LLC2013-09-09HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53439-100-102019-11-27C16284748780-19855d018-e588-cd31-e053-dbdaa90ab51aCut Care Alcohol Prep Pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53439-100-01Cut Care Alcohol Prep Pad1 in 1 POUCHSWAB11
53439-100-10Cut Care Alcohol Prep Pad100 in 1 CARTONSWAB1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53439-100CUT CARE ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) SWAB [ZEUS MEDICAL HOLDINGS LLC]1Legacy NDC, 2 package rows20130915_4f3a151c-9544-4fbe-9ff0-1be625b843ed.zip

DailyMed Socrata Ingredients#

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 44 of 44 · 863 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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
cda8f72f-d34c-4a2d-8762-24ff2717311b4f3a151c-9544-4fbe-9ff0-1be625b843ed2013-09-09WarningsExact identifier
spl id: cda8f72f-d34c-4a2d-8762-24ff2717311b
spl set id: 4f3a151c-9544-4fbe-9ff0-1be625b843ed

Reported adverse events (FAERS/openFDA)#

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