NeuroFreeze

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
NeuroFreeze
Generic name
MENTHOL
Manufacturer
Blue Heron Pharmaceuticals, LLC
Product type
HUMAN OTC DRUG
SPL set ID
bb8aba0a-2378-4eb5-b51e-22957586480b
SPL ID
53f232d7-6507-406c-8a2c-e702350592c8
Version
1
Effective date
2026-02-23
Source export date
2026-11-06
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/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:45:29
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. Do not use on wounds or damaged skin or with a heat source. If pregnant or breastfeeding, ask a healthcare professional before use. When using this product: Avoid bandaging tightly Avoid contact with eyes Keep out of the reach of children

Reported adverse events (FAERS/openFDA)#

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