NeuroMed Topical Analgesic
Tetracaine HCL · Cream · Topical
Active ingredient
Active Ingredients Tetracaine HCL 2.0% w/w
Purpose
Purpose External Analgesic
Uses
Uses For temporary relief of pain and itching due to minor skin irritation
Warnings
For external use only Avoid contact with eyes
Do not use
Do not use in large quantities, particularly over raw surfaces or blistered areas
Stop use and ask a doctor
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.
Keep out of reach of children
Keep out of reach of children
• If product is swallowed, get medical help or contact a Poison Control Center right away.
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.
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?
Questions or Comments? FDA Registered: NDC No. 54723-667-03 800-759-6876
Label text from the FDA structured product label by Sambria Pharmaceuticals, Inc. (revised Nov 12, 2025). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Tetracaine Hydrochloride in 1 product
NeuroMed Topical Analgesic NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 54723-310 | Tetracaine Hydrochloride 20 mg/1000mg Cream | Sambria Pharmaceuticals, Inc. | OTC MONOGRAPH DRUG |
Frequently asked questions
What is NeuroMed Topical Analgesic used for?
Uses For temporary relief of pain and itching due to minor skin irritation
Who makes NeuroMed Topical Analgesic?
NeuroMed Topical Analgesic is listed by 1 labeler in the FDA NDC directory, including Sambria Pharmaceuticals, Inc..