Brazzers Anal Desensitizing Cream

Manufacturer
Metro Media Ent | Bath Concept Cosmetics (Dongguan) Co., Ltd
Effective date
2023-11-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:59:26

Label at a glance#

ProductBrazzers Anal Desensitizing
Active ingredientLIDOCAINE
Label structure7 sections

Dosage and administration

Cleanse affected area with mild soap and water. Gently dry before application. Apply externally to the affected area up to 6 times daily.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 2%

Purpose

OTC - PURPOSE SECTION

Anorectal

Use (s)

INDICATIONS & USAGE SECTION

For temporary relief of pain, soreness or burning in the peritanal area.

Warnings:

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

this product with a mechanical device. Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor. Do not apply onto cracked or broken skin. 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of any bleeding, discontinue use and consult a doctor. As with any drug, consult a health care professional.

Directions

DOSAGE & ADMINISTRATION SECTION

Cleanse affected area with mild soap and water. Gently dry before application. Apply externally to the affected area up to 6 times daily.

Other Information:

SPL UNCLASSIFIED SECTION

  • Store at room temperture 68-77 °F (20-25 °C).
  • Do not use if temper evident seal on the outside of the container is broken or missing.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Dimethicone, Cetearyl Alcohol, Caprylic/Capric Triglyceride, Lidocaine, Glyceryl Stearate, Propylene Glycol, Ceteareth-20, 1,2-Hexanediol, Hydroxyacetophenone, Dimethiconal, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Sodium Hydroxide.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Pharmacologic Classes#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83553-001-00Brazzers Anal Desensitizing29.6 mL in 1 BOTTLECREAM29.63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83553-001BRAZZERS ANAL DESENSITIZING (LIDOCAINE) CREAM [METRO MEDIA ENT]3Current NDC, 1 package rows20231108_ceacd80c-0dd6-4e21-97da-56da877b1c90.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83553-00183553-001-00

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
Brazzers Anal DesensitizingLIDOCAINEMetro Media Entceacd80c-0dd6-4e21-97da-56da877b1c902023-11-06WarningsExact identifier
ndc (package): 83553-001-00
ndc (product): 83553-001
ndc11 (package): 83553000100
spl id: 098692be-efb6-5175-e063-6394a90a1ac2
spl set id: ceacd80c-0dd6-4e21-97da-56da877b1c90

Reported adverse events (FAERS/openFDA)#

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