Lidozall Pro
- Dosage form
- CREAM
- Labeler
- V2 Pharma LLC
- Label updated
- 2026-06-16
- Retrieved
- 2026-09-07
- Active ingredients
- See original label
Lidozall Pro
Rapid-onset topical analgesic
Lidozall Pro should be administered under the supervision of a licensed medical practitioner.
Active Ingredients
Lidocaine HCL 4.0% w/w
Purpose
External analgesic
Uses
For temporary relief of pain and itching due to minor skin irritations.
Warnings
- For external use only.
- Avoid contact with eyes.
Label information
- Do not use in large quantities, particularly over raw surfaces or blistered areas.
Label information
- Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Discontinue use.
Label information
- Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions
For adults and children two-years or older: Apply 1 packet (2 grams) topically to the affected area(s) up to 4 times daily as needed for pain. Do not use more than 4 packets (8 grams) per day.
Inactive Ingredients
Aqua (Deionized Water), Arnica Montana Floweri Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmenthane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine.
Other Information
Protect this product from excessive heat and direct sun.
Product Label
Lidozall Pro
72835-445-05
[Image in the official label — see DailyMed source]
DailyMed Set ID: ecc26ba7-4ff6-43e6-bfb9-91a9cbb509ff · Version 1
NDC: 72835-445