neuromed la topical analgesic
3c1e3a1d-f42b-499d-a445-1d1d3dd26c19
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Purpose
External Analgesic
Description
Tetracaine HCL 2.0% w/w
Medication Information
Warnings and Precautions
For external use only
Avoid contact with eyes
Purpose
External Analgesic
Description
Tetracaine HCL 2.0% w/w
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 then 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
uses
For temporary relief of pain and itching due to minor skin irritation
purpose
External Analgesic
Product Label
directions
For adults and children two-years or older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a physician.
other Information
Protect this product from excessive heat and direct sun.
active Ingredients
Tetracaine HCL 2.0% w/w
inactive Ingredients
Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine
questions Or Comments?
FDA Registered: NDC No. 54723-667-03
800-759-6876
Structured Label Content
Warnings and Precautions (34071-1)
For external use only
Avoid contact with eyes
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 then 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
uses (Uses)
For temporary relief of pain and itching due to minor skin irritation
purpose (Purpose)
External Analgesic
Product Label (Product label)
directions (Directions)
For adults and children two-years or older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a physician.
other Information (Other Information)
Protect this product from excessive heat and direct sun.
active Ingredients (Active Ingredients)
Tetracaine HCL 2.0% w/w
inactive Ingredients (Inactive Ingredients)
Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine
questions Or Comments? (Questions or Comments?)
FDA Registered: NDC No. 54723-667-03
800-759-6876
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
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Source: dailymed · Ingested: 2026-02-15T12:03:32.383113 · Updated: 2026-03-14T23:13:35.542610