FDA label 41b2eeef-3b31-69e2-e063-6294a90a7b92

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
16079e84-3ff2-4e3a-9fe2-69fb625c00eb
SPL ID
41b2eeef-3b31-69e2-e063-6294a90a7b92
Version
7
Effective date
2025-10-21
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 05:14:43

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 As with any drug, ask a doctor before use if pregnant or breast feeding. Do not use more than directed. Consult a physician if symptoms persist for more than 72 hours or worsen. swelling increases, rash or fever develops. irritation,pain or rednes persists or worsens. Keep this and all medications out of the reach of children. Do not use if imprinted tamper-evident bottle cap band is broken or missing. In case of an emergency or accidental overdose, contact a medical professional or Poison Control Center immediately. Hyland's may be contacted for emergency information about our products 24 hours, a day 7 days per week at (800) 624-9659.

Reported adverse events (FAERS/openFDA)#

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