FDA.reportPublic FDA data

NDC 17238-900-99 - BioGlo

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
17238-900
Requested NDC
17238-900-99
Package NDCs from labels
17238-900-99, 17238-900-11, 17238-900-30
Manufacturer
HUB Pharmaceuticals, Inc. | OMNI LENS PRIVATE LIMITED | Madhu Instruments Pvt.Ltd.
Effective date
2024-01-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
BIO GLO (fluorescein sodium) stripHUB Pharmaceuticals, Inc. | OMNI LENS PRIVATE LIMITED | Madhu Instruments Pvt.Ltd.2024-01-01HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17238-900-112026-01-29C16284748780-149896155-afd0-586f-e063-e6dba90add90BIO GLO (fluorescein sodium) strip
17238-900-302026-01-29C16284748780-149896155-afd0-586f-e063-e6dba90add90BIO GLO (fluorescein sodium) strip

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17238-900-11BioGlo100 in 1 BOXSTRIP1009
17238-900-30BioGlo300 in 1 BOXSTRIP3009
17238-900-99BioGlo1 mg in 1 PACKETSTRIP19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17238-900BIOGLO (FLUORESCEIN SODIUM) STRIP [HUB PHARMACEUTICALS, INC.]9Legacy NDC, 3 package rows20240110_f72b68c7-a52f-40df-a47d-8e2d8174091d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
17238-900-11EA - Each17238-900c6b6698b-88c1-4277-96a0-8c949c7b8b1512012-07-24
17238-900-30EA - Each17238-90033463b16-cbce-4a9a-a98b-0732164f8ffb12012-07-24
17238-900-99EA - Each17238-90031a423b7-192d-4b1a-887c-6379ee2b657112023-10-16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FLUORESCEIN SODIUMACTIVE INGREDIENT93X55PE38XBIOGLO (FLUORESCEIN SODIUM) STRIP [HUB PHARMACEUTICALS, INC.]1
FLUORESCEINACTIVE MOIETYTPY09G7XIRBIOGLO (FLUORESCEIN SODIUM) STRIP [HUB PHARMACEUTICALS, INC.]1

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 15 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FLUORESCITEFLUORESCEIN SODIUMAlcon, Inc.ebb3883c-71f6-4fd0-a7e6-0ba8e1136dd92026-06-29Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X
FluoresceinFLUORESCEINZydus Lifesciences Limited5c88e2a2-b05c-46f2-9874-c935e4b96a6e2026-06-02Exact identifier
unii: 93X55PE38X
FluoresceinFLUORESCEINZydus Pharmaceuticals USA Inc.19aea137-3f47-4b69-9884-3bff5f79b04a2026-06-02Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X
FluoresceinFLUORESCEINBPI Labs LLC770582e3-c99b-4a02-868c-29309013717e2026-05-01Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X
AK-FLUORFLUORESCEINLong Grove Pharmaceuticals, LLC73511e79-c050-4dc0-aa2f-a79ed320b5b02026-02-26Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X
C20H10Na2O5 Fluorescein Sodium Ophthalmic StripsFLUORESCEIN SODIUMVistamerica USA292abb69-84ad-4f61-e063-6394a90a14472025-06-01Exact identifier
unii: 93X55PE38X
Fluorescein Sodium and Benoxinate HydrochlorideFLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDEBausch & Lomb Americas Inc.f935b5f8-dc6e-4425-a668-968ee3855f512025-05-12Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X
Fluorescein Sodium and Benoxinate HydrochlorideFLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDEBausch & Lomb Incorporated1797c5ef-66c4-4cf8-b62d-b484242be2ee2025-05-12Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X
0e86525e-501b-e995-e063-6294a90a4d9cf72b68c7-a52f-40df-a47d-8e2d8174091d2024-01-01Exact identifier
spl id: 0e86525e-501b-e995-e063-6294a90a4d9c
spl set id: f72b68c7-a52f-40df-a47d-8e2d8174091d
Fluorescein Sodium and Proparacaine HydrochlorideFLUORESCEIN SODIUM AND PROPARACAINE HYDROCHLORIDEAltaire Pharmaceuticals Inc.dae037ad-dcb8-42e6-8996-e575922d76312022-10-28Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X
FLUORESCEINFLUORESCEINHF Acquisition Co LLC, DBA HealthFirstc1ffe119-7fba-940f-e053-2a95a90a7a172021-08-08Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X
Dry Eye TestFLUORESCEIN SODIUMNomax Inc.04866053-f973-471e-b3bc-241fb76303a22019-12-23Exact identifier
unii: 93X55PE38X
GloStripsFLUORESCEIN SODIUMNomax Inc.d06a4432-c76c-4e2a-abec-6bc5b4e82d512019-12-23Exact identifier
unii: 93X55PE38X
GloStripsFLUORESCEIN SODIUMNomax Inc.f5dbf66b-068d-4408-989b-4f29b3c487382019-12-23Exact identifier
unii: 93X55PE38X
ALTAFLUORFLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDEAltaire Pharmaceuticals Inc.54017304-e680-4129-b52a-69cb9810af762017-12-06Warnings, Adverse reactionsExact identifier
unii: 93X55PE38X

Reported adverse events (FAERS/openFDA)#

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