Florravite

Manufacturer
Florrax Pharmacuetical Corp.
Effective date
2024-07-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:59:39

Label at a glance#

ProductFlorravite
Active ingredientPOTASSIUM IODIDE, ASCORBIC ACID, BIOTIN, LEVOMEFOLIC ACID, .ALPHA.-TOCOPHEROL, FERROUS BISGLYCINATE, VITAMIN A, MAGNESIUM OXIDE, PYRIDOXINE, CYANOCOBALAMIN, CALCIUM CARBONATE, CHOLECALCIFEROL, FOLIC ACID
Label structure11 sections

Storage and handling

STORAGE: Store at 20- 25 degree C (68-77 F) excersions permitted to 15 -30 degree C (59-86 F) {See USP controlled Room Temperature} Avoid excessive heat, light and moisture. TAMPER EVIDENT: Do not use if seal is broken or missing. MADE IN USA Distributed by: 888-321-2821 Florrax Pharmaceutical Corp. Terrell TX 7S161 KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN

Label contents#

Full prescribing information#

Description

DESCRIPTION SECTION

Florrvite is a prescription multivitamin/multimineral dietary supplement.

Other Ingredients

INACTIVE INGREDIENT SECTION

Microcrystalline Cellulose, Maltodextrin, Croscarmellose Sodium,®Silicon Dioxide, Stearic Acid, Magnesium Stearate, Film Coating (Hydroxypropyl®Methylcellulose, Polyethylene Glycol, itanium Dioxide, FD&C Blue# 1)

Indications

INDICATIONS & USAGE SECTION

Florrvite is a prescription multivitamin/multi­mineral dietary supplement formulated for the clinical dietary management of a buoptimal nutritional status in patients where advanced folate, vitamin B supplementa­tion, and maintenance of good health is needed.

Contraindications

CONTRAINDICATIONS SECTION

Florrvite is contraindicated in patients with a known hypersensitivity to any of the ingredients.

Precautions

PRECAUTIONS SECTION

Folic acid alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where Vitamin B 12 deficient. Folic acid in doses above 1.0 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress.

ALLERGIES: NONE

Adverse Reactions

ADVERSE REACTIONS SECTION

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 Pharmaceuticals at 800-000-0000.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

One tablet daily or as directed by a physician.

How Supplied

HOW SUPPLIED SECTION

Bottles of 30 Tablets (84460-901-30). Tablet is light blue, oblong.

SPL UNCLASSIFIED SECTION

*Florrax Pharmaceuticals does not represent this products code to be National Drug Code (NDC). Products codes are formatted according to standard industry practice, to meet the formatting requirement by pedigree reporting and supply-chain control including pharmacies.
This products is a prescription-folate with or without other dietary ingredients the - due to increased folate levels increased risk associated with masking B12 deficiency (pernicious anemia) requires administration under the care of a licensed medical practitioner(64 FR 8760). 1-3 the most appropriate way to ensure pedigree reporting consistent with these regulatory guidelines and safety monitoring is to dispense this product only by prescription. This is not an Orange Book product. This product may be administered only under a physician's supervision and all prescriptions using this product shall be pursuant to state statues as applicable. The ingredients, indication or claims of this product are not to be construed to be Drug claims.

1.) Federal register Notice of August 2, 1973 (39 FR 20750)
2.) Federal Register Notice of October 17, 1980 (45 FR 69043, 69044)

3.) Federal register notice of March 5, 1996 (61 FR 8760)

Storage & Handling

STORAGE AND HANDLING SECTION

STORAGE: Store at 20- 25 degree C (68-77 F) excersions permitted to 15 -30 degree C (59-86 F) {See USP controlled Room Temperature} Avoid excessive heat, light and moisture.


TAMPER EVIDENT: Do not use if seal is broken or missing.
MADE IN USA


Distributed by:
888-321-2821
Florrax Pharmaceutical Corp.
Terrell TX 7S161


KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84460-901FLORRAVITE (MULTIVITAMIN) TABLET [FLORRAX PHARMACUETICAL CORP.]1Unmatched20240704_1c35dac7-95a8-6bf7-e063-6394a90a3ba9.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84460-90184460-901-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

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
3a01f646-6bfa-4231-e063-6394a90a7a831c35dac7-95a8-6bf7-e063-6394a90a3ba92025-07-15Adverse reactionsExact identifier
spl set id: 1c35dac7-95a8-6bf7-e063-6394a90a3ba9

Reported adverse events (FAERS/openFDA)#

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