LIDOCAINE

Manufacturer
Sichuan Gumo Brand Management Co.,Ltd
Effective date
2023-04-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:54:44

Label at a glance#

ProductLIDOCAINE
Active ingredientLIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE
Label structure12 sections

Indications and uses

For the temporary relief of local and anorectal itching , discomfortand pain associated with anorectal disorder or anorectal inflammation.

Dosage and administration

Cleanse the affected area. Sensitivity and possible allergy tests advised prior to use Spray sparingly to affected area after thoroughly cleansing. Wait until anesthetic effect occurs . You may reapply to continue numbing effect. apply to the affected area up to 4 times daily. children under 12 years of age: consult a doctor.

Storage and handling

Keep away from direct sunlight or heat. store in room temperature (59-86F/15-30C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine Hcl 5%

Phenylephrine Hcl 0.25%

Purpose

OTC - PURPOSE SECTION

Local Anesthetic

Vasoconstrictor

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of local and anorectal itching , discomfortand pain associated with anorectal disorder or anorectal inflammation.

Warnings

WARNINGS SECTION

Do not use this product if :
pregnant or breastfeeding, ask a health professional before use.
tamper-evident " Do not se this product if seal is broken or missing.
you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty in urination due to enlargement of prostate gland unless directed by a doctor.

Do not use

OTC - DO NOT USE SECTION

Do not use this product if :
pregnant or breastfeeding, ask a health professional before use.
tamper-evident " Do not se this product if seal is broken or missing.
you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty in urination due to enlargement of prostate gland unless directed by a doctor.

When using

OTC - WHEN USING SECTION

When using this product
do not exceed the recommended the daily usage.
certain persons can develop allergic reactions to ingredients in this product.
do nut put this product into the rectum by using finger or any medical device or applicator.
If swallowed, call your Poison Control Center immediately. If condition worsens or does not improve within 7 days, consult a doctor

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if
The symptom being treated does not subside, or if redness, irritation, swelling, pain, or other symptoms develop or increase.

Directions

DOSAGE & ADMINISTRATION SECTION

Cleanse the affected area.
Sensitivity and possible allergy tests advised prior to use Spray sparingly to affected area after thoroughly cleansing. Wait until anesthetic effect occurs . You may reapply to continue numbing effect.
apply to the affected area up to 4 times daily.
children under 12 years of age: consult a doctor.

Other Information

STORAGE AND HANDLING SECTION

Keep away from direct sunlight or heat.
store in room temperature (59-86F/15-30C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Allantoin, Arginline, Benzyl Alcohol, Disodium EDTA , Ethoxydiglycol, Phenoxyethanol, Polysorbate 20, Purified Water, Sodium Benzoate, Sodium Sulfite

Keep Out Of

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children If Swallowed .Get Medical Help Or Contact A Poison Control Center Right Away

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83365-001-0183365-001-01

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83365-002-012024-07-30C16284748780-11030e365-58f4-111a-e063-dadaa90a10e283365-001
83365-002-012024-01-30C16284748780-11030e365-58f4-111a-e063-dadaa90a10e283365-001

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83365-002-01LIDOCAINE141 g in 1 BOXSPRAY1411

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83365-002LIDOCAINE (LIDOCAINE SPRAY) SPRAY [SICHUAN GUMO BRAND MANAGEMENT CO.,LTD]11 package rows20230420_f9a7f08e-9dff-b9d2-e053-6394a90a8582.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83365-00283365-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
f9a7f08e-9e00-b9d2-e053-6394a90a8582f9a7f08e-9dff-b9d2-e053-6394a90a85822023-04-18WarningsExact identifier
spl id: f9a7f08e-9e00-b9d2-e053-6394a90a8582
spl set id: f9a7f08e-9dff-b9d2-e053-6394a90a8582

Reported adverse events (FAERS/openFDA)#

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