Real Time Pain Relief Maxx Topical Analgesic

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 Maxx Topical Analgesic
Generic name: MENTHOL
Manufacturer: REAL TIME PRODUCTS, INC
Product type: HUMAN OTC DRUG
SPL set ID: f45eb95a-2813-4124-bdb0-54e078a8237d
SPL ID: 2019e91f-7c9a-32bb-e063-6294a90ad6ba
Version: 2
Effective date: 2024-08-20
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:54

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Real Time Pain Relief Maxx Topical Analgesic	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		REAL TIME PRODUCTS, INC	openfda.manufacturer_name
ndc	package	84573-517-64	openfda.package_ndc
ndc	package	84573-517-05	openfda.package_ndc
ndc	package	84573-517-07	openfda.package_ndc
ndc	package	84573-517-16	openfda.package_ndc
ndc	package	84573-517-12	openfda.package_ndc
ndc	package	84573-517-04	openfda.package_ndc
ndc	package	84573-517-03	openfda.package_ndc
ndc	product	84573-517	openfda.product_ndc
ndc11	package	84573051716	derived:openfda.package_ndc
ndc11	package	84573051703	derived:openfda.package_ndc
ndc11	package	84573051707	derived:openfda.package_ndc
ndc11	package	84573051764	derived:openfda.package_ndc
ndc11	package	84573051712	derived:openfda.package_ndc
ndc11	package	84573051705	derived:openfda.package_ndc
ndc11	package	84573051704	derived:openfda.package_ndc
rxcui		1148429	openfda.rxcui
spl id		2019e91f-7c9a-32bb-e063-6294a90ad6ba	id
spl set id		f45eb95a-2813-4124-bdb0-54e078a8237d	set_id
unii		L7T10EIP3A	openfda.unii

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 When using this product: Use only as directed Avoid contact with eyes or mucous membrane Do not apply to wounds or damaged skin Do not bandage tightly 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 Redness is present Irritation develops 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.