FDA label 297bb1f7-666f-1ddd-e063-6394a90acc99

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
e91ddbec-c4ad-b80b-e053-2a95a90a3104
SPL ID
297bb1f7-666f-1ddd-e063-6394a90acc99
Version
4
Effective date
2024-12-17
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:38:37

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.