Assured

Manufacturer
Greenbrier International | FRONT PHARMACEUTICAL PLC
Effective date
2017-04-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:31

Label at a glance#

ProductAssured Feminine Anti-itch
Active ingredientBENZOCAINE, RESORCINOL
Label structure10 sections

Indications and uses

■ temporarily relieves itching

Dosage and administration

Adults and children 2 years of age and older: Apply a fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily. Children under 2 years of age: Consult a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 5%

Resorcinol 2%

Purpose

OTC - PURPOSE SECTION

External analgesic

External analgesic

Uses

INDICATIONS & USAGE SECTION

■ temporarily relieves itching

Warnings

WARNINGS SECTION

For external use only

Avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

Do not apply over large areas of the body

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 of age and older: Apply a fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily. Children under 2 years of age: Consult a doctor

Other information

SPL UNCLASSIFIED SECTION

■ Store at room temperature ■ Lot. No. & Exp. Date: See box or see crimp of tube

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cetearyl Alcohol, Diaziolidinyl Urea, Dimethicone, Glyceryl Stearate & Peg 100 Stearate, Hydroxpropyl Bisstearyldimonium Chloride, Methyparaben, Paraffinum Liquidum,Peg 400, Propylparaben, Purified water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
243587benzocaine 5 % / resorcinol 2 % Vaginal CreamPSN1
243587benzocaine 50 MG/ML / resorcinol 20 MG/ML Vaginal CreamSCD1
243587benzocaine 5 % / resorcinol 2 % Vaginal CreamSY1

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
33992-2014-12020-01-31C16284748780-19d75b9d0-8338-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
33992-2014-1AssuredFeminine Anti-itch21 g in 1 TUBECREAM211

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
33992-2014ASSURED FEMININE ANTI-ITCH (BENZOCAINE RESORCINOL) CREAM [GREENBRIER INTERNATIONAL]1Legacy NDC, 1 package rows20170404_4c5a257c-51b9-44c9-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
33992-201433992-2014-1

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
4c5a257c-51ba-44c9-e054-00144ff88e884c5a257c-51b9-44c9-e054-00144ff88e882017-04-04WarningsExact identifier
spl id: 4c5a257c-51ba-44c9-e054-00144ff88e88
spl set id: 4c5a257c-51b9-44c9-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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