Folinex

Manufacturer
Vivera Pharmaceuticals, Inc.
Effective date
2020-02-10
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:32:16

Label at a glance#

ProductFolinex
Active ingredientASCORBIC ACID, METHYLCOBALAMIN, VITAMIN K7, FOLIC ACID
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

FACTS

Folinex™ is an orally administered prescription folate
product for the dietary management of patients with
unique nutritional needs requiring increased folate
levels and other nutritional supplementation.

Folinex™ should be administered under the supervision
of a licensed medical practitioner.

Folinex™ is used for dietary management of patients
with unique nutritional needs requiring increased
folate levels, or are in need of other nutritional
supplementation. Folinex™ can be taken by women
of childbearing age, pregnant women, and lactating
and nonlactating mothers under the supervision of a
licensed medical practitioner.

PRECAUTIONS SECTION

PRECAUTIONS

Tell your doctor if you have: kidney problems or thyroid
disease. This medication should be used as directed
during pregnancy or while breast-feeding. Consult
your doctor about the risks and benefits. Folic acid alone is
improper therapy in the treatment of pernicious anemia
and other megaloblastic anemias where vitamin B12 is
deficient. Folic acid in doses above 0.1 mg daily may
obscure pernicious anemia in that hematologic remission
can occur while neurological manifestations progress.

WARNINGS SECTION

WARNINGS

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.

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION

Usual adult dose is one (1) tablet once or twice daily or as
prescribed by a licensed medical practitioner.*

PREGNANCY SECTION

If you are pregnant or nursing, ask a
healthcare professional.

OTHER SAFETY INFORMATION


KEEP OUT OF THE REACH OF CHILDREN.

Store at 20°-25°C (68°-77°F); excursions permitted
to 15°-30°C (59°-86°F) [See USP Controlled Room
Temperature.] Protect from heat, light and moisture.

Do not use if seal is broken or missing.

HOW SUPPLIED SECTION

Folinex™ capsules are supplied as a solid, opaque,
white, oblong capsule with “916” printed on one
side, dispensed in child-resistant bottles of 30ct
(72380-916-30*).

OTHER SAFETY INFORMATION

* This product is a prescription-folate with or without other dietary
ingredients that – due to increased folate levels (AUG 2 1973 FR
20750), requires an Rx on the label because of increased risk
associated with masking of B12 deficiency (pernicious anemia). Based
on our assessment of the risk of obscuring pernicious anemia, this
product requires licensed medical supervision, an Rx status, and a
National Drug Code (NDC) – or similarly-formatted product code, as
required by pedigree reporting requirements and supply-chain control
as well as – in some cases, for insurance-reimbursement applications.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC# 72380-916-30

VIVERA™
PHARMACEUTICALS

Folinex™

30 Capsules

Dispensed by Prescription Only

Supplement Facts
Serving Size: 1 Capsule       Servings per container: 30
                          Amount Per Serving    %Daily Value
Vitamin C                   500 mg                         555%
(Ascorbic Acid)
Vitamin B12                1 mg                        41,666%
(as Methylcobalamin)
Vitamin K MK7             100 mcg                         83%
Folate                         1700 mcg DFE               425%
                              (1 mg Folic Acid)

Other ingredients: Gelatin, Magnesium
Stearate, Microcrystalline Cellulose, Dicalcium
Phosphate, Silicon Dioxide, Titanium Dioxide

Dosage: Adult dose is one (1) capsule
once or twice daily or as prescribed by a
licensed medical practitioner.

If you are pregnant or nursing, ask a
healthcare professional.

KEEP OUT OF REACH OF CHILDREN

STORAGE: Store at 20°-25°C (68°-77°F);
excusions permitted to 15°-30°C (59°-86°F)
[See USP Controlled Room Temperature.]
Protect from heat, light , and moisture

Manufactured for:
Vivera Pharmaceuticals, Inc.
11100 Greenstone Ave.
Santa Fe Springs, CA 90670

MADE IN THE U.S.A.         REV120519

LOT NO:
EXP. DATE:
MFG. DATE:

3  72389  00004  9

FolinexFolinex

RES

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASCORBIC ACID Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
91c62db0-0295-c81c-d10a-0856c259edd6Product name220200428
d32bc2b8-0bb7-2216-87aa-24639646e202Product name320190619
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72380-916-302021-07-23C16284748780-1c7ccaba7-2823-fd44-e053-dadaa90aa01bFOLINEX TM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72380-916-30Folinex30 in 1 BOTTLECAPSULE302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72380-916FOLINEX (VITAMIN C, VITAMIN B12, VITAMIN K MK7, FOLATE) CAPSULE [VIVERA PHARMACEUTICALS, INC.]2Legacy NDC, 1 package rows20200211_a63b92a5-32a5-4c73-8bf7-cb8b7bc2bf2d.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72380-91672380-916-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
92d760e5-4d0f-4a7a-80f4-16507c125711a63b92a5-32a5-4c73-8bf7-cb8b7bc2bf2d2020-02-10WarningsExact identifier
spl id: 92d760e5-4d0f-4a7a-80f4-16507c125711
spl set id: a63b92a5-32a5-4c73-8bf7-cb8b7bc2bf2d

Reported adverse events (FAERS/openFDA)#

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