TRANSDERM-IQ

Manufacturer
Direct_Rx
Effective date
2019-09-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:00:30

Label at a glance#

ProductTRANSDERM-IQ
Active ingredientCAPSAICIN, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, LIDOCAINE
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

For external use only

use only as directed. Read and follow all directions and warnings on this carton.
avoid contact with eyes and mucous membranes
do not use at the same time as other topical analgesics
do not use on open wounds, cuts, damaged or infected skin
do not use with bandage or heating pad.

Stop use and ask a doctor if

condition worsens
symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding or if you have sensitive skin, ask a health professional before use

INACTIVE INGREDIENT SECTION


Purified Water, Mineral Oil, Isopropyl Myristate, Cetyl Alcohol, Glycerol Monostearate, Stearic Acid, Glycerin, Propylene Glycol, Cetereth-20, Carbomer, Aloe Vera, Disodium EDTA, Dimethicone, Petrolatum, Methylparaben, Triethanolamine, Diazolidinyl Urea, Iodopropynyl Butylcarbamate, Propylparaben, Beeswax, Sodium Carbomer, Phenonip, Triethanolamine.

SPL UNCLASSIFIED SECTION

New Hands Free Applicator

(Quad-5 Ball Roller)

Long Lasting and Soothing Deep Penetrating Action

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


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

OTC - PURPOSE SECTION


Topical analgesic

OTC - ACTIVE INGREDIENT SECTION

Capsaicin 0.0375%

Lidocaine 4%

Menthol 10%

Methyl Salicylate 20%

INDICATIONS & USAGE SECTION


Temporary relief of minor aches and pains of muscles and joints associated with:• simple backache • arthritis • muscle strains • sprains • bruises

DOSAGE & ADMINISTRATION SECTION

Adults 18 years and children 12 years and older:

apply product directly to affected area
product may be used as necessary, but should not be used more than four times per day
wash hands immediately afterwards.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

851-04851-04

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1876751capsaicin 0.0375 % / lidocaine 4 % / menthol 10 % / methyl salicylate 20 % Topical OintmentPSN2
1876751capsaicin 0.000375 MG/MG / lidocaine 0.04 MG/MG / menthol 0.1 MG/MG / methyl salicylate 0.2 MG/MG Topical OintmentSCD2
1876751capsaicin 0.0375 % / lidocaine 4 % / menthol 10 % / methyl salicylate 20 % Topical OintmentSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61919-851-042023-01-30C16284748780-1f386c649-efad-0266-e053-dadaa90a7c1aTRANSDERM-IQ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61919-851-04TRANSDERM-IQ113 g in 1 TUBEOINTMENT1132

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61919-851TRANSDERM-IQ OINTMENT [DIRECT_RX]2Legacy NDC, 1 package rows20190918_8e822dc1-f770-0c86-e053-2a95a90afff5.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61919-851-04GM - Gram61919-851eb7ebf66-8bd1-4b5e-9cf1-6a5e0a31a59212019-08-06
70364-001-04GM - Gram70364-001b114e8f4-8ae7-4905-8313-a7e73c074a0e12019-06-19

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61919-85161919-851-04
70364-001

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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
92484e87-7074-f870-e053-2995a90a3de38e822dc1-f770-0c86-e053-2a95a90afff52019-09-11WarningsExact identifier
spl id: 92484e87-7074-f870-e053-2995a90a3de3
spl set id: 8e822dc1-f770-0c86-e053-2a95a90afff5

Reported adverse events (FAERS/openFDA)#

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