NDC 71344-002-01 - Cold-Fix

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
71344-002
Requested NDC
71344-002-01
Package NDCs from labels
71344-002-01, 71344-002-02
Manufacturer
Seme USA Inc | Santonika Uab
Effective date
2020-12-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cold-Fix - Seme USA Inc | Santonika UabSeme USA Inc | Santonika Uab2020-12-30HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71344-002-022025-11-18C16284748780-1d6a99b3a-01f6-a426-e053-dadaa90af4c24c09516f-28cc-20d4-e054-00144ff8d46c
71344-002-022022-01-28C16284748780-1d6a99b3a-01f6-a426-e053-dadaa90af4c24c09516f-28cc-20d4-e054-00144ff8d46c

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71344-002COLD-FIX (AFFINITY PURIFIED ANTIBODIES TO HUMAN GAMMA INTERFERON) TABLET [SEME USA INC]4Legacy NDC20201231_4c09516f-28cc-20d4-e054-00144ff8d46c.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 1 of 1 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
43de3a63-1d7f-adf8-e063-6394a90a51ca4c09516f-28cc-20d4-e054-00144ff8d46c2025-11-18WarningsExact identifier
spl set id: 4c09516f-28cc-20d4-e054-00144ff8d46c
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U

Reported adverse events (FAERS/openFDA)#

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