Real Time Pain Relief Maxx Topical Analgesic Lotion

Manufacturer
REAL TIME PRODUCTS, INC
Effective date
2024-08-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:17:31

Label at a glance#

ProductReal Time Pain Relief Maxx Topical Analgesic
Active ingredientMENTHOL
Label structure13 sections

Indications and uses

Temporarily relieves minor pain associated with: Arthritis Simple Backache Muscle Strains Sprains Bruises Cramps

Dosage and administration

Adults and Children over 2 years: Apply to affected area. Massage into painful area until thoroughly absorbed into skin. Repeat as necessary, but no more than 4 times daily. Children 2 years or younger: ask a doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.5%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain associated with: Arthritis

  • Simple Backache
  • Muscle Strains
  • Sprains
  • Bruises
  • Cramps

Warnings:

WARNINGS SECTION

For external use only

When using this product:

OTC - WHEN USING SECTION

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:

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 2 years: Apply to affected area. Massage into painful area until thoroughly absorbed into skin. Repeat as necessary, but no more than 4 times daily. Children 2 years or younger: ask a doctor.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Calendula Officinalis Extract, Caprylyl Glycol, Capsaicin, Centaurea Cyanus (Cornflower) Extract, Chamomilla Matricaria (Chamomile) Extract, Chondroitin Sulfate, Coriandrum Sativum (Coriander) Oil, Emu Oil, Glucosamine Sulfate, Glycerin, Hamamelis Virginiana (Witch Hazel) Distillate, Hypericum Perforatum (St.John Wort), Laureth-7, Mentha Piperita (Peppermint) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Salix Alba (Willow) Bark Extract, SD-Alcohol 40B, Sorbitol, Tilia Cordata (Linden) Bark Extract.

Questions?

OTC - QUESTIONS SECTION

877-787-7180

Package Labeling: 88ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: 120ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling: 147.8ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling: 210ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling: 354ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

Package Labeling: 473ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6Label6

Package Labeling: 1893ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label010Label010

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1148429menthol 1.5 % Topical LotionPSN2
1148429menthol 15 MG/ML Topical LotionSCD2
1148429menthol 1.5 % Topical LotionSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84573-517-03Real Time Pain Relief Maxx Topical Analgesic88 mL in 1 TUBELOTION882
84573-517-04Real Time Pain Relief Maxx Topical Analgesic120 mL in 1 TUBELOTION1202
84573-517-05Real Time Pain Relief Maxx Topical Analgesic147.8 mL in 1 TUBELOTION147.82
84573-517-07Real Time Pain Relief Maxx Topical Analgesic210 mL in 1 TUBELOTION2102
84573-517-12Real Time Pain Relief Maxx Topical Analgesic354 mL in 1 TUBELOTION3542
84573-517-16Real Time Pain Relief Maxx Topical Analgesic473 mL in 1 TUBELOTION4732
84573-517-64Real Time Pain Relief Maxx Topical Analgesic1893 mL in 1 BOTTLELOTION18932

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84573-517REAL TIME PAIN RELIEF MAXX TOPICAL ANALGESIC (MENTHOL) LOTION [REAL TIME PRODUCTS, INC]2Current NDC, 7 package rows20240821_f45eb95a-2813-4124-bdb0-54e078a8237d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84573-51784573-517-03, 84573-517-04, 84573-517-05, 84573-517-07, 84573-517-12, 84573-517-16, 84573-517-64

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Real Time Pain Relief Maxx Topical AnalgesicMENTHOLREAL TIME PRODUCTS, INCf45eb95a-2813-4124-bdb0-54e078a8237d2024-08-20WarningsExact identifier
ndc (package): 84573-517-64
ndc (package): 84573-517-05
ndc (package): 84573-517-07
ndc (package): 84573-517-16
ndc (package): 84573-517-12
ndc (package): 84573-517-04
ndc (package): 84573-517-03
ndc (product): 84573-517
ndc11 (package): 84573051716
ndc11 (package): 84573051703
ndc11 (package): 84573051707
ndc11 (package): 84573051764
ndc11 (package): 84573051712
ndc11 (package): 84573051705
ndc11 (package): 84573051704
spl id: 2019e91f-7c9a-32bb-e063-6294a90ad6ba
spl set id: f45eb95a-2813-4124-bdb0-54e078a8237d

Reported adverse events (FAERS/openFDA)#

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