Melt Pain Away

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
Melt Pain Away
Generic name
CAPSAICIN
Manufacturer
Proximity Capital Partners LLC dba Asutra
Product type
HUMAN OTC DRUG
SPL set ID
a95a11d7-a2ae-6654-e053-2a95a90a802c
SPL ID
37da3909-1e23-f5d9-e063-6294a90a8f48
Version
3
Effective date
2025-06-18
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:44:42
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

Use only as directed. For external use only. When using this product: avoid contact with eyes do not apply to wounds or damaged skin do not bandage tightly Stop use and ask doctor if: condition worsens symptoms persist for more than 7 days, or clear up and reoccur again with a few days redness is present irritation develops. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children . If accidentally ingested, get medical help or contact Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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