TRANSDERM IQ

Manufacturer
DIRECT RX
Effective date
2022-10-04
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:52:29

Label at a glance#

ProductTRANSDERM IQ
Active ingredientMENTHOL, UNSPECIFIED FORM, LIDOCAINE
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients:

Lidocaine HCL 4%

Menthol 4%

OTC - PURPOSE SECTION

Purpose:

Topical Anesthetic

INDICATIONS & USAGE SECTION

Uses:

For the temporary relief of pain

WARNINGS SECTION

Warnings:

For external use

OTC - DO NOT USE SECTION

Do not use:

More than 1 patch on your body at a time or on cut, iritated or swollen skin.
On puncture wounds
For more than 1 week without consulting a doctor

OTC - WHEN USING SECTION

When using this product:

Use only as directed. Read and follow all directions and warnings on this label.
Rare cases of serious burns have been reported with products of this type.
Do not apply to wounds or damaged, broken or irritated skin.
Do not allow contact with the eyes and mucous membranes.
Do not bandage tightly or apply local heat (such as heating pads) to the area of use.
Do not use at the same time as other topical analgesics.
Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

OTC - STOP USE SECTION

Stop use and ask a doctor if:

Condition worsens
Redness is present
Irritation developes
Symptoms persist for more than 7 days or clear up and occur again within a few days.
You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.

PREGNANCY SECTION

If pregnant or breast-feeding, ask a health care professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

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

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults and children over 12 years:

Clean and dry the affected area.
Open pouch and remove one patch.
Remove the protective film from the patch and apply patch to the affected area.
Reseal pouch containing unused patches after each use.
Use 1 patch for up to 12 hours.

Children 12 years or younger:

Ask a doctor

OTHER SAFETY INFORMATION

Other Information:

Avoid storing product in direct sunlight
Protect product from excessive mositure

INACTIVE INGREDIENT SECTION

Other Ingredients:

Acrylic Adhesive

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

148148

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

166166

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72189-148-15EA - Each72189-148ccebdf7f-4d27-4745-9266-9b9e1eaf276512021-05-05
70512-013-15EA - Each70512-0132a3dd89e-8aed-4d3a-b817-bba1f2a0e08312021-04-08

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72189-14872189-148-15
70512-013

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LenzaPro FlexLIDOCAINE/MENTHOLSOLA Pharmaceuticalsba498f1d-460b-f4e6-e053-2995a90a57552025-12-08WarningsExact identifier
ndc (product): 70512-013
0bc8f9ba-0cdb-a634-e063-6294a90aac0dea36a884-b247-4306-e053-2a95a90a8ebc2023-12-05WarningsExact identifier
spl set id: ea36a884-b247-4306-e053-2a95a90a8ebc

Reported adverse events (FAERS/openFDA)#

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