NDC 62011-0272-01 - Health Mart Isopropyl Alcohol 91 Percent

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
62011-0272
Requested NDC
62011-0272-01
Package NDCs from labels
62011-0272-1, 62011-0272-01
Manufacturer
Strategic Sourcing Services LLC | Pharma Nobis, LLC
Effective date
2023-12-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Isopropyl Alcohol - Strategic Sourcing Services LLC | Pharma Nobis, LLCStrategic Sourcing Services LLC | Pharma Nobis, LLC2023-12-20HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62011-0272-1Health Mart Isopropyl Alcohol 91 Percent473 mL in 1 BOTTLELIQUID4738

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62011-0272HEALTH MART ISOPROPYL ALCOHOL 91 PERCENT (ISOPROPYL ALCOHOL) LIQUID [STRATEGIC SOURCING SERVICES LLC]8Current NDC, Legacy NDC, 1 package rows20231221_fbd2aa69-b1c7-4a28-9642-a436ae09faaf.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62011-0272-1ML - Milliliter62011-02725f2bc3e9-72c3-4082-8f21-3a900f8b37a412016-11-08

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 130 of 130 · 2,581 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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