FDA.reportPublic FDA data

Altafluor 0.4 % / 0.25 % Ophthalmic Solution

RxCUI
2099522
RxNorm name
Altafluor 0.4 % / 0.25 % Ophthalmic Solution
Display name
Altafluor 0.4 % / 0.25 % Ophthalmic Solution
Full name
Altafluor 0.4 % / 0.25 % Ophthalmic Solution
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:38:58

RxNav Current And Historical NDCs#

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UNII Substances#

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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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ALTAFLUORFLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDEAltaire Pharmaceuticals Inc.54017304-e680-4129-b52a-69cb9810af762017-12-06Warnings, Adverse reactionsExact identifier
rxcui: 2099522

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
54017304-e680-4129-b52a-69cb9810af76Altafluor 0.4 % / 0.25 % Ophthalmic Solution [PSN] · benoxinate hydrochloride 4 MG/ML / fluorescein sodium 2.5 MG/ML Ophthalmic Solution [Altafluor] [SBD] · Altafluor (benoxinate HCl 0.4 % / fluorescein sodium 0.25 % ) Ophthalmic Drops [SY]35These highlights do not include all the information needed to use ALTAFLUOR BENOX safely and effectively. See full prescribing information for ALTAFLUOR BENOX. Altafluor Benox (fluorescein sodium and benoxinate hydrochloride ophthalmic solution) 0.25%/ 0.4% for topical ophthalmic use Initial U.S. Approval: 201720171206