FREEZE IT Menthol Roll On 3.5 g/100mL
Menthol · GEL · LiquidCapsule Manufacturing LLC
FREEZE IT Menthol Roll On is a gel containing menthol at 3.5 g/100mL, taken topical. Manufactured by LiquidCapsule Manufacturing LLC.
Key Facts
- Brand Name
- FREEZE IT Menthol Roll On
- Generic Name
- Menthol
- NDC Code (Product)
71726-005- Manufacturer
- LiquidCapsule Manufacturing LLC
- Strength
- 3.5 g/100mL
- Dosage Form
- GEL
- Route
- TOPICAL
- Marketing Status
- Application #
- M017
- Marketing Start
- 06/05/2025
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses Temporarily relieves minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains
Dosage & Administration
Directions adults and children 12 years of age and older: rub a thin film over affected area not more than 3 to 4 times daily children under 2 years of age: consult a physician wash hands after use with cool water
Warnings
Warnings For external use only. Flammable: Keep away from excessive heat or open flame
Frequently Asked Questions
What is FREEZE IT Menthol Roll On used for?
FREEZE IT Menthol Roll On contains Menthol. It is a gel taken topical. Consult your doctor for specific uses.
Is FREEZE IT Menthol Roll On a controlled substance?
FREEZE IT Menthol Roll On is not classified as a controlled substance by the DEA.
What is the generic name for FREEZE IT Menthol Roll On?
The generic name for FREEZE IT Menthol Roll On is Menthol. There are 12 other brand versions of Menthol.
What is the NDC code for FREEZE IT Menthol Roll On 3.5 g/100mL?
The NDC (National Drug Code) for FREEZE IT Menthol Roll On 3.5 g/100mL is 71726-005, listed by LiquidCapsule Manufacturing LLC.
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)