lidozall
1eb2dfb2-3ad1-488b-aed9-17220e34a10c
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Purpose
External analgesic
Description
Rapid-onset topical analgesic
Medication Information
Warnings
- For external use only.
- Avoid contact with eyes.
Uses
For temporary relief of pain and itching due to minor skin irritations.
Purpose
External analgesic
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.
Other Information
Protect this product from excessive heat and direct sun.
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.
Description
Rapid-onset topical analgesic
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
Lidozall
Rapid-onset topical analgesic
Active Ingredients
Lidocaine HCL 4.0% w/w
Structured Label Content
Warnings
- For external use only.
- Avoid contact with eyes.
Uses
For temporary relief of pain and itching due to minor skin irritations.
Purpose
External analgesic
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.
Other Information
Protect this product from excessive heat and direct sun.
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.
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)
Lidozall
Rapid-onset topical analgesic
Active Ingredients
Lidocaine HCL 4.0% w/w
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
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Source: dailymed · Ingested: 2026-02-15T12:06:37.855001 · Updated: 2026-03-14T23:13:35.542610