Lidozall

Lidozall
SPL v4
SPL
SPL Set ID 1eb2dfb2-3ad1-488b-aed9-17220e34a10c
Route
TOPICAL
Published
Effective Date 2025-07-25
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Inactive Ingredients
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

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2024-11-21

Description

Rapid-onset topical analgesic

Purpose

External analgesic


Medication Information

Purpose

External analgesic

Description

Rapid-onset topical analgesic

Uses

For temporary relief of pain and itching due to minor skin irritations.

Section 42229-5

Lidozall Box of 20 Count, 2 Gram Packets

NDC 72835-004-20

Section 50565-1

- Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9

- 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.

Section 50570-1

- Do not use in large quantities, particularly over raw surfaces or blistered areas.

Section 51945-4

Warnings

- For external use only.

- Avoid contact with eyes.

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.

Lidozall 

Rapid-onset topical analgesic

Other Information

Protect this product from excessive heat and direct sun.

Active Ingredients

Lidocaine HCL 4.0% w/w

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.


Structured Label Content

Uses

For temporary relief of pain and itching due to minor skin irritations.

Section 42229-5 (42229-5)

Lidozall Box of 20 Count, 2 Gram Packets

NDC 72835-004-20

Section 50565-1 (50565-1)

- Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9 (50566-9)

- 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.

Section 50570-1 (50570-1)

- Do not use in large quantities, particularly over raw surfaces or blistered areas.

Section 51945-4 (51945-4)

Purpose

External analgesic

Warnings

- For external use only.

- Avoid contact with eyes.

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.

Lidozall 

Rapid-onset topical analgesic

Other Information

Protect this product from excessive heat and direct sun.

Active Ingredients

Lidocaine HCL 4.0% w/w

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.


Advanced Ingredient Data


Raw Label Data

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