Indications and uses
For temporary relief of pain and itching due to minor skin irritations.
Lidozall Pro
- Manufacturer
- V2 Pharma LLC
- Effective date
- 2026-06-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-07-15 00:32:59
Label at a glance#
ProductLidozall Pro
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure11 sections
Dosage and administration
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.
Label contents#
Full prescribing information#
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.
OTC - DO NOT USE SECTION
- Do not use in large quantities, particularly over raw surfaces or blistered areas.
OTC - STOP USE SECTION
- 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.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
- 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
Products#
Every source-derived product name is available through these pages.
- Lidozall Pro
- LIDOCAINE HYDROCHLORIDE
- ARNICA MONTANA FLOWER
- WATER
- C13-14 ISOPARAFFIN
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW)
- EMU OIL
- DIETHYLENE GLYCOL MONOETHYL ETHER
- ETHYLHEXYLGLYCERIN
- GLUCOSAMINE SULFATE
- ISOPROPYL PALMITATE
- MELALEUCA ALTERNIFOLIA LEAF
- DIMETHYL SULFONE
- PHENOXYETHANOL
- PROPYLENE GLYCOL
- STEARIC ACID
- TROLAMINE
- LIDOCAINE
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72835-445 | 72835-445-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lidozall Pro | LIDOCAINE HYDROCHLORIDE | V2 Pharma LLC | ecc26ba7-4ff6-43e6-bfb9-91a9cbb509ff | 2026-06-16 | Warnings | 72835-445-05 72835-445 72835044505 ef3aeded-ab30-4b42-ab71-d5aa7c0fbd60 ecc26ba7-4ff6-43e6-bfb9-91a9cbb509ff |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.