MYDERM PRO FREEZE SPOT STICK CONCENTRATED PAIN RELIEF FORMULA 15.75 MENTHOL- menthol stick

MyDerm Pro Freeze spot stick concentrated pain relief formula 15.75 menthol by

Drug Labeling and Warnings

MyDerm Pro Freeze spot stick concentrated pain relief formula 15.75 menthol by is a Otc medication manufactured, distributed, or labeled by Inspec Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Menthol 15.75%

WHEN USING

When using this product avoid contact with the eyes or mucous membranes do not apply to wounds or damaged skin do not apply to irritated skin do not bandage wash hands after use with cool water do not use with heating pad or device.

WARNINGS

For external use only.

STOP USE

Stop use and ask doctor if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days.

PURPOSE

Menthol 15.75%------------------------------------------------Topical Analgesic

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Apply to affected area not more than 3 to 4 times a day

INDICATIONS & USAGE

For external use only

INACTIVE INGREDIENT

Inactive Ingredients:

Inactive Ingredients:

Purified Water

Ethyl alcohol

ISOPROPYL MYRISTATE

Acetone

Methanol

Acetaldehyde

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MYDERM PRO FREEZE SPOT STICK CONCENTRATED PAIN RELIEF FORMULA 15.75 MENTHOL 
menthol stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72667-074
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, (+)- (UNII: C6B1OE8P3W) (MENTHOL, (+)- - UNII:C6B1OE8P3W)	MENTHOL, (+)-	15.75 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ACETALDEHYDE (UNII: GO1N1ZPR3B)
ALCOHOL (UNII: 3K9958V90M)
METHYL ALCOHOL (UNII: Y4S76JWI15)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72667-074-01	19 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/06/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/06/2024

Labeler - Inspec Solutions (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions		081030372	manufacture(72667-074)