Indications and uses
For temporary relief of pain and itching due to minor skin irritations.
Lidozall
- Manufacturer
- V2 Pharma LLC | Southeast Holdings Corp
- Effective date
- 2025-11-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 01:43:25
Label at a glance#
ProductLidozall
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
Rapid-onset topical analgesic
Lidozall 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.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
SPL UNCLASSIFIED SECTION
Lidozall Box of 20 Count, 2 Gram Packets
NDC 72835-004-20
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| LIDOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 070fbed5-7088-434a-a7ce-f2a64d8d40ac | Product name | 2 | 20260107 |
| bee66ce1-adb7-9d3b-67d9-582e4c54e80f | Product name | 5 | 20250819 |
| 860a93dc-4863-49cc-b284-6bbe8191bc48 | Product name | 4 | 20250214 |
| eaba870a-6a9d-442e-8643-87b3f558a451 | Product name | 1 | 20250117 |
| 9b4cf230-fd05-41d5-98c6-5db9ecb27b86 | Product name | 1 | 20230117 |
| 7d755fa1-1087-4dcd-98f0-6d4bba479a57 | Product name | 3 | 20210602 |
| aed701d5-9c75-dfaf-7154-cde46179faea | Product name | 9 | 20200313 |
| fa8b5901-e681-426f-82fe-54f6d81ec698 | Product name | 4 | 20180619 |
| 332d03e4-aa24-4b11-841a-02bf41081920 | Product name | 1 | 20171221 |
| c08ab52f-2fc8-4409-9d9f-ed8edc0bd070 | Product name | 1 | 20171221 |
| 68ed98f8-24c2-44a0-944a-6d36e82ce25a | Product name | 1 | 20141222 |
| 1cd42bc2-a430-c72b-636d-991b235fbf80 | Product name | 1 | 20140508 |
| 49fa150c-f0de-cce7-3d9c-993ed81c5698 | Product name | 1 | 20140508 |
| 4d7ae718-ed00-bae8-2abe-9eaec1eef7ff | Product name | 1 | 20140508 |
| 9137811f-f279-8640-5aeb-99fa2145d64d | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72835-004-01 | Lidozall | 2 g in 1 PACKET | CREAM | 2 | 4 | |
| 72835-004-20 | Lidozall | 20 in 1 CARTON | CREAM | 20 | 4 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72835-004-01 | GM - Gram | 72835-004 | 0e4be1af-3198-4174-80d4-bd8446bcd125 | 1 | 2025-01-14 |
| 72835-004-20 | GM - Gram | 72835-004 | 406714f4-2d24-4070-a7cd-2e36cd5503d0 | 1 | 2025-01-14 |
Products#
Every source-derived product name is available through these pages.
- Lidozall
- 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 |
|---|---|
| 72835-004 | 72835-004-01, 72835-004-20 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 2 | 2025-07-25 | full-release | 2026-06-01 01:08:38 |
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 | LIDOCAINE HYDROCHLORIDE | V2 Pharma LLC | 1eb2dfb2-3ad1-488b-aed9-17220e34a10c | 2025-11-12 | Warnings | 72835-004-20 72835-004-01 72835-004 72835000401 72835000420 436cebe5-b978-2a2f-e063-6294a90a7227 1eb2dfb2-3ad1-488b-aed9-17220e34a10c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.