FDA.reportPublic FDA data

GLONOINUM

Product NDC
15631-2758
11-digit product format
156312758
Labeler code
15631
Product ID
15631-2758_19ce7c40-f956-33ba-e063-6394a90aa554
Type
HUMAN OTC DRUG
Nonproprietary name
GLONOINUM
Dosage form
LIQUID
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-05-23
Substance
NITROGLYCERIN
Active strength
6 [hp_X]/mL
Pharmacologic classes
Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GLONOINUM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NITROGLYCERIN6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
G59M7S0WS3Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
19ce76ed-ce59-1214-e063-6394a90a6b77Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
00358076-c817-430b-b924-11d717dc307cProduct name120160718
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-2758-0GLONOINUM10 mL in 1 BOTTLELIQUID101
15631-2758-1GLONOINUM30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-2758GLONOINUM LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Current NDC, 2 package rows20240602_19ce76ed-ce59-1214-e063-6394a90a6b77.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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GLONOINUMGLONOINUMRxhomeo Private Limited d.b.a. Rxhomeo, Inc19ce76ed-ce59-1214-e063-6394a90a6b772024-06-01WarningsExact identifier
ndc (product): 15631-2758

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
15631-2758-01563127580010 mL in 1 BOTTLE (15631-2758-0) 10 ml2024-05-23NoNoCurrent
15631-2758-11563127580130 mL in 1 BOTTLE (15631-2758-1) 30 ml2024-05-23NoNoCurrent