NDC 70963-003-01 - FLUIDBASE RETINOL VIT C

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
70963-003
Requested NDC
70963-003-01
Package NDCs from labels
70963-003-01, 70963-003-02
Manufacturer
LABORATORIO GENOVE S.A. | LABORATORIO GENOVE S A
Effective date
2016-10-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
FLUIDBASE RETINOL VIT C - LABORATORIO GENOVE S.A. | LABORATORIO GENOVE S ALABORATORIO GENOVE S.A. | LABORATORIO GENOVE S A2016-10-20HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70963-003-022020-02-13C16284748780-19d75b9d0-e5c9-f424-e053-dadaa90a57ceFLUIDBASE RETINOL VIT C
70963-003-022020-01-31C16284748780-19d75b9d0-e5c9-f424-e053-dadaa90a57ceFLUIDBASE RETINOL VIT C

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 · 864 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ARGAN AIR WATER BANG ESSENCEDIMETHICONEPioom Cosmetic Co.,ltd34e79668-0710-5753-e054-00144ff88e882016-06-08WarningsExact identifier
unii: 92RU3N3Y1O
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
AntacidALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE AND SIMETHICONESafewayd36b56a4-06f0-47ff-8add-4c327d60be222016-01-21WarningsExact identifier
unii: 92RU3N3Y1O
Gas ReliefSIMETHICONESafeway14a9fb00-707a-4b55-a060-82ad53a806e32016-01-08WarningsExact identifier
unii: 92RU3N3Y1O

Reported adverse events (FAERS/openFDA)#

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