ScleraCare Lidocaine HCL 3% Gel

Manufacturer
ScleraCare, LLC
Effective date
2020-03-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:39:24

Label at a glance#

ProductScleraCare Lidocaine HCL
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure8 sections

Indications and uses

• For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites or minor skin irritations.

Dosage and administration

• Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. • Children under two-years of age: consult a physician.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Lidocaine hydrochloride 3.00%

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Uses:

INDICATIONS & USAGE SECTION

• For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites or minor skin irritations.

Warnings:

WARNINGS SECTION

• For external use only not intended for ingestion.

When using this product

OTC - WHEN USING SECTION

• Avoid contact with eyes

Do not use 

OTC - DO NOT USE SECTION

• in large quantities, particularly over raw surfaces or blistered areas

Stop use and ask a doctor if

OTC - STOP USE SECTION

symptoms persist for more than seven days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• If swallowed, get medical help or contact a Poinson Control Center right away.
• Do not apply to wounds or damaged skin.
• Do not bandage tightly.
• If pregnant or breast feeding, contact physician prior to use.

Directions:

DOSAGE & ADMINISTRATION SECTION

• Adults and children two-years of age or older: Apply to affected area not more than three to four times daily.
• Children under two-years of age: consult a physician.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

a-Bisabalol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Butylene Glycol, Cucumis Sativus (Cucumber) Fruit Extract, Ethylhexylglycerin, Opuntia Vulgaris (Prickly Pear) Extract, Persea gratissima (Avocado) Oil, Phenoxyethanol, Polysorbate-20, Sodium Alginate, Squalane, Triethanolamine.

Other Information:

SPL UNCLASSIFIED SECTION

• Store at room temperature

Question?

OTC - QUESTIONS SECTION

337-526-6744 (M-F) (9-5pm EST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73698-10673698-106-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
074b4425-6be0-352c-e063-6394a90ac59e550df5b8-52cd-4bca-b19d-f40ce050e8932023-10-09WarningsExact identifier
spl set id: 550df5b8-52cd-4bca-b19d-f40ce050e893

Reported adverse events (FAERS/openFDA)#

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