Fast Freeze Pain Relieving

Generic: MENTHOL, UNSPECIFIED FORM

Over-the-Counter DrugTOPICAL

Drug Information

Brand Name
Fast Freeze Pain Relieving
Generic Name
MENTHOL, UNSPECIFIED FORM
Manufacturer
NATURAL ESSENTIALS, INC.
Product Type
Over-the-Counter Drug
Route
TOPICAL
Application Number
15a26af1-ca5a-40fc-a411-6c0e8ae18fbb

Active Ingredients

Indications & Usage

Uses Temporary relief of minor aches and pains of muscles and joints associated with: Simple backache Arthritis Strains Sprains

Warnings

Warnings For external use only Flammable Keep away from excessive heat or open flame Do not use With heating pad or device With ointments, creams, sprays or liniments On wounds, damaged skin or irritated skin Ask a doctor before use if you Have sensitive skin Are pregnant or breastfeeding When using this product Avoid contact with eyes or mucous membranes Do not bandage tightly Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up then reoccur again wit...

Read full warnings

Warnings For external use only Flammable Keep away from excessive heat or open flame Do not use With heating pad or device With ointments, creams, sprays or liniments On wounds, damaged skin or irritated skin Ask a doctor before use if you Have sensitive skin Are pregnant or breastfeeding When using this product Avoid contact with eyes or mucous membranes Do not bandage tightly Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up then reoccur again within a few days Irritation develops Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Adverse Reactions

No specific warnings reported by FDA for this product.

Medical Disclaimer: This information is for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare provider before making any decisions about your medications. Data sourced from openFDA.

Fast Freeze Pain Relieving - Side Effects, Warnings, Uses | FDA Drug Database