Indications and uses
For temporary relief of pain and itching due to minor skin irritation
For temporary relief of pain and itching due to minor skin irritation
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.
Tetracaine HCL 2.0% w/w
External Analgesic
For temporary relief of pain and itching due to minor skin irritation
For external use only
Avoid contact with eyes
Do not use in large quantities, particularly over raw surfaces or blistered areas
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
• If product is swallowed, get medical help or contact a Poison Control Center right away.
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.
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
Protect this product from excessive heat and direct sun.
FDA Registered: NDC No. 54723-667-09
800-759-6876
| Class | Version | Type | Effective |
|---|---|---|---|
| TETRACAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| a26f29b9-6919-4f09-a354-491df8d2b97d | Product name | 1 | 20251021 |
| 122d1fa8-7b9e-49b4-89ce-b062ffd1d947 | Product name | 1 | 20181030 |
| a993dfc5-f219-4460-bde6-30dd724d9ef0 | Product name | 1 | 20160818 |
| 4d7ae718-ed00-bae8-2abe-9eaec1eef7ff | Product name | 1 | 20140508 |
| 9137811f-f279-8640-5aeb-99fa2145d64d | Product name | 1 | 20140508 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 54723-669-09 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-12cf-fd44-e053-dadaa90aa01b | Eclipse LL Topical Analgesic |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54723-669-09 | Eclipse Topical AnalgesicLL | 1500 mg in 1 PACKET | CREAM | 1500 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 54723-669 | 54723-669-09 |
Every source-derived ingredient row is available through these pages.
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| a3801b6f-fc54-4ad9-88c0-2dc968ab75cb | 6e0e3594-0c69-495e-9972-13af2773c88d | 2018-08-06 | Warnings | a3801b6f-fc54-4ad9-88c0-2dc968ab75cb 6e0e3594-0c69-495e-9972-13af2773c88d |
Adverse event summaries are temporarily unavailable. Other product information remains available.