FDA.reportPublic FDA data

Instaflex Pain Relief Cream

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Instaflex Pain Relief Cream
Generic name
MENTHOL
Manufacturer
Adaptive Health, LLC
Product type
HUMAN OTC DRUG
SPL set ID
911f5021-a851-444e-8c2a-2be4fa94e828
SPL ID
e7dfe524-438c-45e8-b652-fa625f72bc79
Version
1
Effective date
2018-12-21
Source export date
2026-08-01
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/928e480b2a9ec5fd356ebc3e5dcca70f0f57b8a051cfbb174a4421de39bb77a2/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:24:33
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use with a heating pad, may blister skin on open wounds or damaged skin Ask a doctor before use if you have redness over the affected area When using this product Use only as directed avoid contact with eyes do not bandage tightly Stop use and ask a doctor if skin redness or excessive skin irritation develops condition worsens or symptoms persist for more than 7 days symptoms clear up and occur again in a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.