FDA.reportPublic FDA data

MyDerm Pro Freeze spot stick concentrated pain relief formula 15.75 menthol

Manufacturer
Inspec Solutions
Effective date
2024-06-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:14:25

Label at a glance#

ProductMyDerm Pro Freeze spot stick concentrated pain relief formula 15.75 menthol
Active ingredientMENTHOL, (+)-
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Menthol 15.75%

OTC - WHEN USING SECTION

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 SECTION

For external use only.

OTC - STOP USE SECTION

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.

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

INDICATIONS & USAGE SECTION

For external use only

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Inactive Ingredients:

Purified Water

Ethyl alcohol

ISOPROPYL MYRISTATE

Acetone

Methanol

Acetaldehyde

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Myderm pro Freeze spot stickMyderm pro Freeze spot stick

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72667-074MYDERM PRO FREEZE SPOT STICK CONCENTRATED PAIN RELIEF FORMULA 15.75 MENTHOL (MENTHOL) STICK [INSPEC SOLUTIONS]2Unmatched20240630_13003e39-5e38-5f74-e063-6394a90aebf1.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72667-07472667-074-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, (+)-C6B1OE8P3WACTIB
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ACETALDEHYDEGO1N1ZPR3BIACT
ALCOHOL3K9958V90MIACT
METHYL ALCOHOLY4S76JWI15IACT

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
47f68962-ffe3-6dd8-e063-6294a90ad3ca13003e39-5e38-5f74-e063-6394a90aebf12026-01-09WarningsExact identifier
spl set id: 13003e39-5e38-5f74-e063-6394a90aebf1

Reported adverse events (FAERS/openFDA)#

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