FDA label 7c616198-2d98-4a8e-9fe0-2a1bf618a08a

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)

SPL set ID
8b23f206-43eb-454b-9608-b9cb985209cd
SPL ID
7c616198-2d98-4a8e-9fe0-2a1bf618a08a
Version
3
Effective date
2018-12-14
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:52:16

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: VP-GGR-B6 contains ginger. Ginger may increase the risk of bleeding in certain situations. Individuals with bleeding disorders and/or those receiving anti-coagulant therapy or anti-platelet therapy should ask their licensed medical practitioner before using this product. In addition, those individuals undergoing surgery should seek advice of their medical practitioner. Individuals with cardiac conditions, gallstones, diabetes and/or hypoglycemia should consult their medical practitioner before taking this product. See product ingredients. Please consult your healthcare practitioner or pharmacist for more information.

Adverse reactions cross-check#

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

adverse reactions

ADVERSE REACTIONS: Allergic sensitization has been reported following both oral and parental administration of folic acid, and may possibly occur with other forms of folate. Paresthesia, somnolence, nausea and headaches have been reported with vitamin B 6 . Gas, bloating, heartburn, and nausea have been associated with ginger, but normally with high doses.

Reported adverse events (FAERS/openFDA)#

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