TRANSDERM IQ by DIRECT RX Transderm IQ

TRANSDERM IQ by

Drug Labeling and Warnings

TRANSDERM IQ by is a Otc medication manufactured, distributed, or labeled by DIRECT RX. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TRANSDERM IQ- transderm iq patch 
DIRECT RX

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Transderm IQ

Active ingredients:

Lidocaine HCL 4%

Menthol 4%

Purpose:

Topical Anesthetic

Uses:

For the temporary relief of pain

Warnings:

For external use

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

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.

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.

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

Keep out of reach of children and pets.

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

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 Information:

Avoid storing product in direct sunlight
Protect product from excessive mositure

Other Ingredients:

Acrylic Adhesive

TRANSDERM IQ 
transderm iq patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72189-148(NDC: 70512-013)
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	40 mg  in 1 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
POLYOXYL 100 STEARATE (UNII: YD01N1999R)
DIMETHICONE 350 (UNII: 2Y53S6ATLU)
TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
ALOE (UNII: V5VD430YW9)
CETYL ALCOHOL (UNII: 936JST6JCN)
ALLANTOIN (UNII: 344S277G0Z)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color		Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72189-148-15	15 in 1 BOX	04/07/2021	12/06/2023
1		1 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	04/07/2021	12/06/2023

Labeler - DIRECT RX (079254320)

Registrant - DIRECT RX (079254320)

Establishment
Name	Address	ID/FEI	Business Operations
DIRECT RX		079254320	relabel(72189-148)

Revised: 12/2023

Document Id: 0bc8f9ba-0cdb-a634-e063-6294a90aac0d

34390-5

Set id: ea36a884-b247-4306-e053-2a95a90a8ebc

Version: 9

Effective Time: 20231205