FDA label 297ba442-32f3-bd95-e063-6394a90aca2a

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
ef305eef-6d2a-f687-e053-2995a90ae173
SPL ID
297ba442-32f3-bd95-e063-6394a90aca2a
Version
3
Effective date
2024-12-17
Source export date
2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:34:54

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

Broadway Joe's Pain Cream Warnings · For external use only. Do not use on open wounds or damaged skin or with a heating pad. When using this product · avoid contact with eyes or mucous membranes. If product contacts your eyes, rinse thoroughly with water. Do not bandage tightly. · Do not use with other ointments, creams, or sprays. Stop use and ask a doctor if you experience redness or excessive skin irritation over the affected area. · If the condition worsens, or symptoms persist for more than 7 days please consult a Dr. Keep out of reach of children . If swallowed, seek medical help, or contact a Poison Control Center immediately. If pregnant or breast feeding , ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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