FDA.reportPublic FDA data

Real Time Pain Relief Foot

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
Real Time Pain Relief Foot
Generic name
MENTHOL
Manufacturer
Real Time Products Inc.
Product type
HUMAN OTC DRUG
SPL set ID
29c8e06d-9b29-44f9-ac21-9160d06475cb
SPL ID
1dfa79de-8251-2efc-e063-6394a90ab5ac
Version
1
Effective date
2024-07-24
Source export date
2026-08-17
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-17/58bbe7c9ef0bbcdd26f1198c312a74ec14e12ccd9d56bd49878542e8f7ce071c/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 08:31:04
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: Do not apply to wounds or damaged skin or bandage tightly. For external use only. When using this product: Avoid contact with eyes. Stop use and ask doctor if: Condition worsens Symptoms persist for more than 7 days or 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. If pregnant or breast-feeding, ask a health professional before use.