FDA label 6a9c6a8e-d26a-369d-e053-2a91aa0a5c33

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
6a9c55a3-bc73-1eb9-e053-2a91aa0a3e54
SPL ID
6a9c6a8e-d26a-369d-e053-2a91aa0a5c33
Version
1
Effective date
2018-04-24
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:28:48

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Folic Acid alone is improper treatment of pernicious anemia and other megaloblastic anemias where Vitamin B12 is deficient.

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 rarely following oral and parenteral administration of Folic Acid. At recommended doses, Nicotinamide, Zinc Oxide, Cupric Acid, Folic Acid Tablets is expected to be well tolerated. Gastrointestinal distress such as nausea or vomiting have been associated with the administration of Nicotinamide or zinc at doses greater than the recommended dose.

Reported adverse events (FAERS/openFDA)#

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