NEUROFLEX Topical Pain Relieving Liquid

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
NEUROFLEX Topical Pain Relieving Liquid
Generic name
CAMPHOR (SYNTHETIC), MENTHOL
Manufacturer
Almark Products Inc
Product type
HUMAN OTC DRUG
SPL set ID
6da3aa84-7a01-4041-8792-a4bbf49e6e4e
SPL ID
09d72589-142c-349f-e063-6294a90a4d95
Version
2
Effective date
2023-11-10
Source export date
2026-10-27
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 19:48:53
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 Flammable: Keep away from fire or flame. Do not use • on wounds • on damaged skin • on mucous membranes When using this product • avoid contact with eyes • do not bandage tightly • do not use a heating pad Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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