Anti-Itch Cream

Manufacturer
Walgreens | Anicare Pharmaceuticals Pvt. Ltd
Effective date
2022-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:24

Label at a glance#

ProductAnti-Itch Regular Strength
Active ingredientBENZOCAINE, RESORCINOL
Label structure9 sections

Dosage and administration

adults and children 12 years and older apply a fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily. clean nozzle of tube by wiping thoroughly before replacing cap. Keep cap tightly closed between uses. children under 12 years 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

Use

INDICATIONS & USAGE SECTION

Temporarily relieves itching

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

Avoid contact with eyes

OTC - STOP USE SECTION

Stop use and ask doctor if 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.

Do not use if allergic to any of the ingredients

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. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 years and older

  • apply a fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily.
  • clean nozzle of tube by wiping thoroughly before replacing cap. Keep cap tightly closed between uses.

children under 12 years

  • consult a doctor

Other information

SPL UNCLASSIFIED SECTION

store at 20°-25°C (68°-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract, carbomer, cetyl alcohol, cholecalciferol, glyceryl stearate, isopropyl myristate, isopropyl palmitate, isopropyl stearate, lanolin, methylparaben, mineral oil, PEG-100 stearate, propylene glycol, retinyl palmitate, sodium hydroxide, sodium sulfite, tocopheryl acetate, trisodium  HEDTA, water

Questions or comments

SPL UNCLASSIFIED SECTION

1-800-WALGREEN (1-800-925-4733)

Principal display panel - 28 g Carton Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0363-0621-02

REGULAR STRENGTH

Anti-Itch Cream

Pain Relieving Cream

NET WT 1 OZ (28 g)

label of anti-itch
label of anti-itch

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
243587benzocaine 5 % / resorcinol 2 % Vaginal CreamPSN2
243587benzocaine 50 MG/ML / resorcinol 20 MG/ML Vaginal CreamSCD2
243587benzocaine 5 % / resorcinol 2 % Vaginal CreamSY2

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-0621-022024-01-30C16284748780-11030e365-34a7-111a-e063-dadaa90a10e2Anti-Itch Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0621-02Anti-ItchRegular Strength1 in 1 CARTONCREAM12
0363-0621-02Anti-ItchRegular Strength28 g in 1 TUBECREAM282

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0621ANTI-ITCH REGULAR STRENGTH (BENZOCAINE AND RESORCINOL) CREAM [WALGREENS]2Legacy NDC, 2 package rows20220123_64bc4ad7-4081-4f0e-9642-8e86705356d1.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-06210363-0621-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
d6280ea7-ddfd-a97d-e053-2a95a90a407d64bc4ad7-4081-4f0e-9642-8e86705356d12022-01-22WarningsExact identifier
spl id: d6280ea7-ddfd-a97d-e053-2a95a90a407d
spl set id: 64bc4ad7-4081-4f0e-9642-8e86705356d1

Reported adverse events (FAERS/openFDA)#

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