Truu Balance Pain Relief
- Dosage form
- CREAM
- Labeler
- Philia Group LLC
- Label updated
- 2020-08-13
- Retrieved
- 2026-09-07
- Active ingredients
- MENTHOL, UNSPECIFIED FORM
Label information
Drug Facts
유효 성분
성분·작용
| Active Ingredients | Purpose |
|---|---|
| Lidocaine 4% HCl w/w | External Analgesic |
| Menthol 1% w/w | External Analgesic |
Uses
For temporary relief of pain, burning, or itching where applied locally
Warnings
For eternal use only
Avoid contact with eyes
Label information
Do not use in large quantities, particularly over raw surfaces or blistered areas
Stop use and ask Doctor if
- Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days.
Label information
Keep out of reach of children
- If product is swallowed get medical help or contact a Poison Control Center right away.
- This product is not intended to diagnose, treat, cure or prevent any disease
Directions
Apply in a circular motion for 30 to 60 seconds
For adults and children two-years and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a physician.
Inactive ingredients
Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine, Full Spectrum Hemp Extract. (Aerial Parts)
Other Information
Protect this product from excessive heat and direct sunlight
Questions or Comments
FDA Registered: NDC No. _____-___-__
Label information
Distributed by Philia Group LLC
Address: 4 Flanders Drive, Pine Brook, NJ 07058
PRINCIPAL DISPLAY PANEL - 113 g Bottle Label
Truu
Balance
Pain Relief Cream
Organic Full Spectrum CBD
With lidocaine
THIRD PARTY
LAB TESTED
1000mg CBD
4oz | 113g
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[Image in the official label — see DailyMed source]
DailyMed Set ID: 62290685-c67e-4aa4-8a95-c17b49886d36 · Version 1
NDC: 73596-100