Capsaicin Heat

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
Capsaicin Heat
Generic name
CAPSAICIN
Manufacturer
Universal Distribution Center LLC
Product type
HUMAN OTC DRUG
SPL set ID
b3b40f77-3b0b-4111-968b-f3a87a5701fa
SPL ID
03f572e2-8835-4d7f-af61-714a0f4da238
Version
7
Effective date
2025-09-29
Source export date
2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:42:38
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: EXTERNAL USE ONLY DO NOT USE • on wounds or damaged skin • with a heating pad • with or at the same times as other external analgesic • if you are allergic to any ingredients of this product When using this product • do not use otherwise than as directed • avoid contact with the eyes, mucous membranes or rashes • do not bandage tightly • discontinue use at least 1 hour before a bath or shower • do not use immediately after a bath or shower STOP USE and ask a doctor if • rash, itching or excessive skin irritation develops • conditions worsen • symptoms persist for more than 7 days • symptoms clear up and occur again within few days If pregnant or breast-feeding , ask a health professional before use. KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Reported adverse events (FAERS/openFDA)#

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