FDA.reportPublic FDA data

FDA label 2b60e482-9ba3-c178-e063-6294a90a14c9

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
f398f8bd-12a8-41e1-9ec5-9f542f84b881
SPL ID
2b60e482-9ba3-c178-e063-6294a90a14c9
Version
3
Effective date
2025-01-10
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:15:57

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 For external use only. May be harmful if swallowed. Allergy Alert Do not use if allergic to any ingredients in VitaStem™ ULTRA. Do not use in eyes over large areas of the body longer than 1 week unless directed by doctor Ask a doctor before use if you have deep or punture wounds animal bites serious trauma Stop use and ask a doctor if condition persists or gets worse. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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