Norvexa Mini

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Norvexa Mini
Generic name: NORVEXA MINI
Manufacturer: Florrax Pharmaceutical
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 7c964ffd-4b14-43ef-9163-db21c6a1afc6
SPL ID: 6ea9aff5-fa44-48b0-9df4-b7b0e9a800d9
Version: 1
Effective date: 2026-04-27
Source export date: 2026-10-30
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:10:15

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Norvexa Mini	openfda.brand_name
generic name		NORVEXA MINI	openfda.generic_name
manufacturer name		Florrax Pharmaceutical	openfda.manufacturer_name
ndc	package	84460-911-30	openfda.package_ndc
ndc	product	84460-911	openfda.product_ndc
ndc11	package	84460091130	derived:openfda.package_ndc
spl id		6ea9aff5-fa44-48b0-9df4-b7b0e9a800d9	id
spl set id		7c964ffd-4b14-43ef-9163-db21c6a1afc6	set_id
unii		R5L488RY0Q	openfda.unii
unii		935E97BOY8	openfda.unii
unii		PQ6CK8PD0R	openfda.unii
unii		81G40H8B0T	openfda.unii
unii		P6YC3EG204	openfda.unii
unii		1C6V77QF41	openfda.unii
unii		X66NSO3N35	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Accidental overdose of iron-containing products is a leading cause of fatal poising in children under 6. KEEP THIS PRODUCT OUT OF REACH OF CHILDREN. In the case of accidental overdose, call a doctor or poison control center immediately.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTIONS Allergic sensitization has been reported following both oral and parenteral administration of folic acid. You should call your doctor for medical advice about serious adverse events. To reports adverse side effects or to obtain product information, contact Florrax Pharma at 888-321-2821.

Reported adverse events (FAERS/openFDA)#

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