FDA.reportPublic FDA data

Lidoease™ 2% Gel

Manufacturer
PureTek Corporation
Effective date
2026-04-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:54:07

Label at a glance#

ProductLidoease 2%
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure8 sections

Indications and uses

For the temporarily relief of pain and itching associated with: ■ minor burns ■ sunburn ■ minor cuts ■ scrapes ■ insect bites ■ minor skin irritations

Dosage and administration

■ Adults and children 2 years or older: Apply to affected area not more than 3 to 4 times daily. ■ Children under 2 years: do not use; consult a licensed healthcare practitioner.

Storage and handling

■ Store at 20°-25°C (68°-77°F) [See USP controlled room temperature].Protect from freezing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 2%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporarily relief of pain and itching associated with:
■ minor burns ■ sunburn ■ minor cuts ■ scrapes ■ insect bites ■ minor skin irritations

Warnings

WARNINGS SECTION

For external use only.

When using this product:

OTC - WHEN USING SECTION

■ Avoid contact with the eyes. ■ Do not use in large quantities, particularly over raw surfaces or blistered areas.

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use and consult a licensed healthcare practitioner.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

■ Adults and children 2 years or older: Apply to affected area not more than 3 to 4 times daily.
■ Children under 2 years: do not use; consult a licensed healthcare practitioner.

Other information

STORAGE AND HANDLING SECTION

■ Store at 20°-25°C (68°-77°F) [See USP controlled room temperature].Protect from freezing.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (Aloe Vera) Leaf Juice, Aqua (Purified Water), Caprylyl Glycol, Carbomer, Chlorphenesin, Cucumis Sativus (Cucumber) Fruit Extract, Dimethicone, Glycerin, Phenoxyethanol, Propanediol, Propylene Glycol, Sodium Hydroxide.

Lidoease™ 2% Gel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3 oz (85 g)
LabelLabel

1 oz (28.35 g)
labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1011852lidocaine HCl 2 % Topical GelPSN2
1011852lidocaine hydrochloride 0.02 MG/MG Topical GelSCD2
1011852lidocaine hydrochloride 2 % Topical JellySY2

DailyMed Pharmacologic Classes#

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130359088221037GTIN-13: 0359088221037
EAN-13: 0359088221037
GTIN-12: 359088221037
UPC-A: 359088221037
GTIN storage (14 digits): 00359088221037		1 oz label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59088-221-03Lidoease 2%28.35 g in 1 TUBEGEL28.352
59088-221-07Lidoease 2%85 g in 1 TUBEGEL852

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59088-221-03GM - Gram59088-221b7d6c353-5566-4310-b073-6ab086436caa12026-05-22
59088-221-07GM - Gram59088-2213b2ba2ca-d6b0-4b1a-86ee-ddd5725c7f1012025-09-12

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59088-22159088-221-07, 59088-221-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
CARBOMER0A5MM307FCIACT
CUCUMBERYY7C30VXJTIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
CHLORPHENESINI670DAL4SZIACT
GLYCERINPDC6A3C0OXIACT
PROPANEDIOL5965N8W85TIACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT

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
Lidoease 2%LIDOCAINE HCL 2%PureTek Corporation3ba0c0ff-0f7a-7a29-e063-6294a90a547a2026-04-16WarningsExact identifier
ndc (package): 59088-221-03
ndc (package): 59088-221-07
ndc (product): 59088-221
ndc11 (package): 59088022103
ndc11 (package): 59088022107
spl id: 4f9c0791-9946-ef1f-e063-6394a90ad7e1
spl set id: 3ba0c0ff-0f7a-7a29-e063-6294a90a547a

Reported adverse events (FAERS/openFDA)#

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