Eclipse Topical Analgesic

Manufacturer
Sambria Pharmaceuticals, Inc. | A.I.G. Technologies, Inc. | JP Packaging LLC
Effective date
2018-08-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:02:24

Label at a glance#

ProductEclipse Topical Analgesic LL
Active ingredientTETRACAINE HYDROCHLORIDE
Label structure12 sections

Indications and uses

For temporary relief of pain and itching due to minor skin irritation

Dosage and administration

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.  Apply in a circular motion for 30 to 60 seconds.

Label contents#

Full prescribing information#

​Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Tetracaine HCL     2.0% w/w

​Purpose

OTC - PURPOSE SECTION

External Analgesic

​Uses

INDICATIONS & USAGE SECTION

For temporary relief of pain and itching due to minor skin irritation

WARNINGS SECTION

​For external use only

Avoid contact with eyes

OTC - DO NOT USE SECTION

​Do not use​ in large quantities, particularly over raw surfaces or blistered areas

OTC - STOP USE SECTION

​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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

​Keep out of reach of children​

• If product is swallowed, get medical help or contact a Poison Control Center right away.

​Directions

DOSAGE & ADMINISTRATION SECTION

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.  Apply in a circular motion for 30 to 60 seconds.

​Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

​Other Information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

​Questions or Comments?

OTC - QUESTIONS SECTION

FDA Registered: NDC No. 54723-669-05

800-759-6876

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packetpacket

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1543158tetracaine HCl 2 % Topical CreamPSN3
1543158tetracaine hydrochloride 20 MG/ML Topical CreamSCD3
1543158tetracaine HCl 2 % Topical CreamSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
TETRACAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a26f29b9-6919-4f09-a354-491df8d2b97dProduct name120251021
122d1fa8-7b9e-49b4-89ce-b062ffd1d947Product name120181030
a993dfc5-f219-4460-bde6-30dd724d9ef0Product name120160818
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54723-669-052021-07-23C16284748780-1c7ccaba7-24cc-fd44-e053-dadaa90aa01bEclipse LL Topical Analgesic

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54723-669-05Eclipse Topical AnalgesicLL5 mg in 1 PACKETCREAM53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54723-669ECLIPSE TOPICAL ANALGESIC LL (TETRACAINE HCL) CREAM [SAMBRIA PHARMACEUTICALS, INC.]3Legacy NDC, 1 package rows20191227_bb67a8d2-8799-4672-ac4a-a9124f1f543f.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54723-66954723-669-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e00eb06a-8aab-45be-8df6-e179544750b4bb67a8d2-8799-4672-ac4a-a9124f1f543f2018-08-06WarningsExact identifier
spl id: e00eb06a-8aab-45be-8df6-e179544750b4
spl set id: bb67a8d2-8799-4672-ac4a-a9124f1f543f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.