Eclipse Topical Anesthetic
7e060d95-c161-4823-b5ad-f93145020134
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Description
Lidocaine HCL 4.00% w/w
Purpose
External Analgesic
Medication Information
Purpose
External Analgesic
Description
Lidocaine HCL 4.00% w/w
Uses
For temporary relief of pain and itching due to minor skin irritation.
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 to affected area not more than 3 or 4 times daily. Children under 2 years of age: consult a physician. Apply in a circular motion for 50 to 60 seconds.
Active Ingredient
Lidocaine HCL 4.00% w/w
Inactive Ingredients
Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chrondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexyglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine.
other Information
Protect this product from excessive heat and direct sun.
questions Or Comments?
FDA Registered: NDC No. 54723-667-04
800-759-6876
Structured Label Content
Uses
For temporary relief of pain and itching due to minor skin irritation.
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 to affected area not more than 3 or 4 times daily. Children under 2 years of age: consult a physician. Apply in a circular motion for 50 to 60 seconds.
Active Ingredient
Lidocaine HCL 4.00% w/w
Inactive Ingredients
Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chrondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexyglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine.
other Information (Other Information)
Protect this product from excessive heat and direct sun.
questions Or Comments? (Questions or Comments?)
FDA Registered: NDC No. 54723-667-04
800-759-6876
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
Back to search View SPL set listing Open on DailyMed ↗
Source: dailymed · Ingested: 2026-02-15T11:56:58.853232 · Updated: 2026-03-14T22:55:48.069158