FDA.reportPublic FDA data

Norvexa Mini

Product NDC
84460-911
11-digit product format
844600911
Labeler code
84460
Product ID
84460-911_6ea9aff5-fa44-48b0-9df4-b7b0e9a800d9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Norvexa Mini
Dosage form
TABLET
Route
ORAL
Labeler
Florrax Pharmaceutical
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2026-04-27
Substance
VITAMIN A; ASCORBIC ACID; CHOLECALCIFEROL; THIAMINE; FOLIC ACID; CYANOCOBALAMIN; FERROUS FUMARATE
Active strength
1000; 100; 1000; 20; 1.67; 100; 27 [iU]/1; mg/1; [iU]/1; mg/1; mg/1; ug/1; mg/1
Pharmacologic classes
Ascorbic Acid [CS], Vitamin A [CS], Vitamin A [EPC], Vitamin B 12 [CS], Vitamin B12 [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Norvexa Mini
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VITAMIN A1000 [iU]/1
ASCORBIC ACID100 mg/1
CHOLECALCIFEROL1000 [iU]/1
THIAMINE20 mg/1
FOLIC ACID1.67 mg/1
CYANOCOBALAMIN100 ug/1
FERROUS FUMARATE27 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
81G40H8B0TInternal UNII lookup
PQ6CK8PD0RInternal UNII lookup
1C6V77QF41Internal UNII lookup
X66NSO3N35Internal UNII lookup
935E97BOY8Internal UNII lookup
P6YC3EG204Internal UNII lookup
R5L488RY0QInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
7c964ffd-4b14-43ef-9163-db21c6a1afc6Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cf050ccd-1144-f76a-e00d-e5698d8597d4Product name620250625
b82b4008-22fd-05f5-6cc6-c0a6e81c65b8Product name220240805
91c62db0-0295-c81c-d10a-0856c259edd6Product name220200428
d32bc2b8-0bb7-2216-87aa-24639646e202Product name320190619
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
d206bb34-ea65-399d-70d9-834f22dc2c18Product name320170724
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84460-911-30Norvexa Mini1 in 1 BOTTLETABLET11

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
Norvexa MiniNORVEXA MINIFlorrax Pharmaceutical7c964ffd-4b14-43ef-9163-db21c6a1afc62026-04-27Warnings, Adverse reactionsExact identifier
ndc (product): 84460-911

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84460-911-30844600911301 TABLET in 1 BOTTLE (84460-911-30) 1 tablet2026-04-27NoNoCurrent