Toast Screamin Hot

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)

Brand name
Toast Screamin Hot
Generic name
CAPSAICIN
Manufacturer
IDEAZ, LLC
Product type
HUMAN OTC DRUG
SPL set ID
331207e6-b8ac-b169-e063-6394a90ac169
SPL ID
45c8fc9d-bea5-c36e-e063-6294a90af22a
Version
2
Effective date
2025-12-12
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:16:58
Harmonized routes table
Harmonized routes
TOPICAL

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: TEST FIRST ON A SMALL AREA OF SKIN TO DETERMINE SENSITIVITY. When using this product ■ use only as directed ■ do not bandage tightly ■ do not use with a heating pad ■ avoid contact with the eyes and mucus membranes ■ do not apply to wounds, damaged, broken or rritated skin ■ a slight burning sensation may occur upon application but generally disappears in several days ■ if burning occurs, discontinue use ■ do not expose the treated area to heat or direct sunlight ■ do not use if allergic to capsicum or chili peppers. Stop using consult a doctor if ■ condition worsens ■ symptoms persist for more than 7 days or clear up and occur again within a few days ■ redness is present ■ irritation develops. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately. If pregnant or breast-feeding ask a healthcare professional before use.

Reported adverse events (FAERS/openFDA)#

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