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
2026-09-28
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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:52
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 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.