BEAUELI

Manufacturer
EUbizrival LLC | Guangzhou Pallas Cosmetics Co.,Ltd.
Effective date
2023-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:55:56

Label at a glance#

ProductBEAUELI
Active ingredientLIDOCAINE
Label structure8 sections

Indications and uses

For the temporary relief of local and anorectal itching and discomfort associated with anorectal disorders.

Dosage and administration

When practical clean area with mild soap and warm water and rinse thoroughly. Gently dry by patting or bloating with toilet tissue or soft cloth before applying. Adults and children 12 years and older: apply externally to the affected area up to 6 times a day. Children under 12 years of age: consult a doctor To use finger cots: roll one finger cot over finger. Gently squeeze cream on to finger cot. Smooth a layer ...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5%

Purpose

OTC - PURPOSE SECTION

Local Anesthetic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of local and anorectal itching and discomfort associated with anorectal disorders.

Warnings

WARNINGS SECTION

For external use only

When using this product

  • Do not get into eyes.
  • Do not exceed recommend dosage unless directed by doctor.
  • Do not put this product into rectum by using fingers or any mechanical device or applicator.

Stop use and ask a doctor if

  • condition worsens or does not improve within 7 days.
  • allergic reaction occurs to ingredients in this product.
  • symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase.
  • symptoms clear up and return within a few days.

Keep out of reach of children.If swallowed, get medical help. Do not use if allergic to any ingredients.

If pregnant or breastfeedingask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • When practical clean area with mild soap and warm water and rinse thoroughly. Gently dry by patting or bloating with toilet tissue or soft cloth before applying.
  • Adults and children 12 years and older: apply externally to the affected area up to 6 times a day.
  • Children under 12 years of age: consult a doctor
  • To use finger cots: roll one finger cot over finger. Gently squeeze cream on to finger cot. Smooth a layer of the cream.

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature. Avoid direct sunlight. Do not use if temper evident packaging has been breached or is missing.

INACTIVE INGREDIENT SECTION

water, glycerine, Lidocaine Lsopropyl palmitate, Aloe barbadensis leaf juice, Retinol,Helianthus annuus (sunflower)seed oil, Glyceryl stearate,
Pentylene glycol, Butyrospermum parkii (shea)butter,Cetyl alcohol, Piper methysticum leaf/root/stem extract, Peg-100 stearate, Tocopheryl acetate.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1366789lidocaine 5 % Rectal CreamPSN1
1366789lidocaine 50 MG/ML Rectal CreamSCD1
1366789lidocaine 5 % Rectal CreamSY1

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83462-001-012025-01-30C16284748780-11030e365-61f5-111a-e063-dadaa90a10e2f725ecd1-96de-4f9f-94c9-d22c676285b2
83462-001-012024-01-30C16284748780-11030e365-61f5-111a-e063-dadaa90a10e2f725ecd1-96de-4f9f-94c9-d22c676285b2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83462-001-01BEAUELI50 g in 1 BOTTLECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83462-001BEAUELI (LIDOCAINE) CREAM [EUBIZRIVAL LLC]11 package rows20230819_f725ecd1-96de-4f9f-94c9-d22c676285b2.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
83462-00183462-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
03339501-199f-81bc-e063-6294a90aac3ef725ecd1-96de-4f9f-94c9-d22c676285b22023-08-18WarningsExact identifier
spl id: 03339501-199f-81bc-e063-6294a90aac3e
spl set id: f725ecd1-96de-4f9f-94c9-d22c676285b2

Reported adverse events (FAERS/openFDA)#

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