FDA Label for Tuvivex
View Indications, Usage & Precautions
Tuvivex Product Label
The following document was submitted to the FDA by the labeler of this product Tuvive Therapeutics. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Other
Drug Facts
Active Ingredient
Menthol 4%
Purpose
Topical Analgesic
Uses
Aid for temporary local relief of minor pain in muscles or joints.
Warnings
- For external use only.
- Avoid contact with eyes.
- Do not apply to wounds or damaged skin.
- If symptoms persist for more than seven days, discontinue use and consult a physician.
If Pregnant Or Breastfeeding
Ask a health professional before use.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help right away.
Directions
Adults and children two years of age or older:
- Apply to affected area not more than three to four times daily.
- Children under two years of age, consult a physician.
Additional Information
Store in a cool, dry ptace at 20 to 25 C (68 to77 F) with lid closed tightly.
Inactive Ingredients
Aqua, Alcohol Denat, Steareth-21, Glycerin, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol, Hemp-Derived Cannabidiol (CBD), Arnica Montana Flower Extract, Steareth-2, Cetyl Alcohol, Xanthan Gum, Boswellia Serrata Extract.
Otc - Questions
To report a serious adverse event or to obtain product information, contact Company number at 1-844-720-7251
Principal Display Panel - 90 Ml Bottle Label
Tuvīve
Therapeutics
73501-500-90
Tuvīvex™
Menthol 4% Roll on Gel
with CBD
Roll On
Pain Gel
CBD
500MG
Per Bottle
3 fl. oz (90 mL)
* Please review the disclaimer below.