Cobalefol

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
Cobalefol
Generic name
VITAMIN
Manufacturer
V2 Pharma LLC
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
7d409065-112d-4bc7-bae6-d558aeb7c0e4
SPL ID
9a9099c2-4b67-4e39-9bd3-924ae7a4e667
Version
1
Effective date
2025-05-16
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:18:51
Harmonized routes table
Harmonized routes
ORAL

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 KEEP COBALEFOL OUT OF THE REACH OF CHILDREN. In case of accidental overdose, call a licensed medical practitioner or poison control center immediately. For use under the supervision of a licensed medical practitioner. Consult your physician prior to using Cobalefol if you are pregnant, nursing, taking medication, or have a medical condition.

Reported adverse events (FAERS/openFDA)#

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