Folcyteine

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: Folcyteine
Generic name: MULTIVITAMIN
Manufacturer: PureTek Corporation
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 04cf0026-e29b-ffd5-e063-6294a90aca1f
SPL ID: 5592f382-e77e-a812-e063-6294a90a905c
Version: 2
Effective date: 2026-07-08
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:06

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Folcyteine	openfda.brand_name
generic name		MULTIVITAMIN	openfda.generic_name
manufacturer name		PureTek Corporation	openfda.manufacturer_name
ndc	package	59088-795-54	openfda.package_ndc
ndc	product	59088-795	openfda.product_ndc
ndc11	package	59088079554	derived:openfda.package_ndc
spl id		5592f382-e77e-a812-e063-6294a90a905c	id
spl set id		04cf0026-e29b-ffd5-e063-6294a90aca1f	set_id
unii		935E97BOY8	openfda.unii
unii		WYQ7N0BPYC	openfda.unii
unii		1C6V77QF41	openfda.unii
unii		MLM29U2X85	openfda.unii
unii		RHO26O1T9V	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 : Patients with kidney disease or thyroid disease should consult a physician or healthcare provider before using this product. Use during pregnancy or breast-feeding only as directed. Administration of folic acid alone is improper therapy for pernicious anemia and other megaloblastic anemias caused by vitamin B12 deficiency.

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. To report side effects, call PureTek Corporation at 1-877-921-7873 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Reported adverse events (FAERS/openFDA)#

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