NDC 79681-004 - disinfecting wipes

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
79681-004
Package NDCs from labels
79681-004-01, 79681-004-02, 79681-004-03, 79681-004-04, 79681-004-05, 79681-004-06
Manufacturer
Fuan HnH Bio Tech Co., Ltd.
Effective date
2020-07-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
disinfecting wipes - Fuan HnH Bio Tech Co., Ltd.Fuan HnH Bio Tech Co., Ltd.2020-07-26HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79681-004-01disinfecting wipes30 in 1 BAGCLOTH301
79681-004-02disinfecting wipes50 in 1 BAGCLOTH501
79681-004-03disinfecting wipes70 in 1 BAGCLOTH701
79681-004-04disinfecting wipes70 in 1 CANISTERCLOTH701
79681-004-05disinfecting wipes100 in 1 CANISTERCLOTH1001
79681-004-06disinfecting wipes160 in 1 CANISTERCLOTH1601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79681-004DISINFECTING WIPES (ALCOHOL) CLOTH [FUAN HNH BIO TECH CO., LTD.]16 package rows20200727_ab63d52b-0a7f-c98b-e053-2995a90a23ed.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 9 of 9 · 162 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.