Ultimate Topical Pain Relief Patch
CAPSAICIN and MENTHOL, UNSPECIFIED FORM · Patch · Topical
Active ingredient
Active Ingredients Menthol 5.00% Capsaicin 0.0375%
Purpose
Purpose: External Analgesic/Counterirritant External Analgesic/Counterirritant
Uses
Directions Adults and children 12 and over apply to affected area; change patch 1 to 2 times daily Children under 12 years: Consult physician before use.
Warnings
Warnings For external useonly. Avoid contact with eyes and mucous membranes. Do not use on wounds or damaged skin. Do not cover with bandage. Do not use if you are allergic to Menthol. Consult physician for use on children under 12. Stop use and ask a doctor if conditions worsen, if symptoms persist for more than 7 days or clear up and occur again with a few days, or if a rash, itching or excessive skin irritation occurs. If pregnant or breast feeding ask a health professional before use. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
Ask a doctor before use
Stop use and ask a doctor if conditions worsen, if symptoms persist for more than 7 days or clear up and occur again with a few days, or if a rash, itching or excessive skin irritation occurs.
Pregnancy or breast-feeding
If pregnant or breast feeding ask a health professional before use.
Keep out of reach of children
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Dosage and Administration Ultimate Topical Pain Relief Patch contains 0.0375% capsaicin and 5.00% menthol
Other information
Other Information Store below 25°C (77°F). Avoid direct sunilght.
Inactive ingredients
Inactive Ingredients: Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Diazolidinyl Urea, EDTA Disodium ,Glycerin, Iodopropynyl Butylcarbamate, Methylparaben, Polysorbate 80, Propylparaben, Sodium Polyacrylate, and Water.
Questions?
Questions or Comments? Please call 1-800-290-6816 (Mon-Fri 9AM-5PM CST)
Label text from the FDA structured product label by Foshan Aqua Gel Biotech Co.,Ltd. (revised Nov 6, 2017). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Menthol, Unspecified Form in 1 product
- Capsaicin in 1 product
Ultimate Topical Pain Relief Patch NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 69159-910 | Menthol, Unspecified Form 5 g/100g; Capsaicin .0375 g/100g Patch | Foshan Aqua Gel Biotech Co.,Ltd. | OTC MONOGRAPH NOT FINAL |
Frequently asked questions
What is Ultimate Topical Pain Relief Patch used for?
Directions Adults and children 12 and over apply to affected area; change patch 1 to 2 times daily Children under 12 years: Consult physician before use.
Who makes Ultimate Topical Pain Relief Patch?
Ultimate Topical Pain Relief Patch is listed by 1 labeler in the FDA NDC directory, including Foshan Aqua Gel Biotech Co.,Ltd..