NDC 71878-040-01 - ARMIYOU HYDROGEN

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
71878-040
Requested NDC
71878-040-01
Package NDCs from labels
71878-040-01, 71878-040-02
Manufacturer
Armiyou
Effective date
2017-11-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ARMIYOU HYDROGEN - ArmiyouArmiyou2017-11-22HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71878-040-022021-01-29C16284748780-1ba0f9c33-22e5-a910-e053-dadaa90a0b85d213c8ae-c6c9-4fb6-8a4c-f9285582d0bb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71878-040-01ARMIYOU HYDROGEN50 mL in 1 CONTAINERCREAM501
71878-040-02ARMIYOU HYDROGEN1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71878-040ARMIYOU HYDROGEN (NIACINAMIDE, ADENOSINE) CREAM [ARMIYOU]1Legacy NDC, 2 package rows20171122_d213c8ae-c6c9-4fb6-8a4c-f9285582d0bb.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 21 of 21 · 402 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

Reported adverse events (FAERS/openFDA)#

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