Well at Walgreens Anti-Itch

Manufacturer
Anicare Pharmaceuticals Pvt. Ltd
Effective date
2020-12-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:39

Label at a glance#

ProductWell at Walgreens Anti-Itch Maximum Strength
Active ingredientBENZOCAINE, RESORCINOL
Label structure8 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 children under 12 years consult a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 20%

Resorcinol 3%

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

When using this product avoid contact with eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Also, do not use if you have an unusual or abnormal vaginal discharge except under the supervision of a physician.

Do not apply over large areas of the body.

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.

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

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 vera gel, carbomer, cetyl alcohol, corn oil, disodium EDTA, fragrance, glyceryl stearate, isopropyl myristate, isopropyl palmitate, lanolin, methyl-4 hydroxybenzoate, mineral oil, PEG-100 stearate, propylene glycol, purified water, stearic acid, stearyl alcohol, triethanolamine, vitamin A, E & D

Principal display panel - 28 g Carton Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Well at Walgreens

WALGREENS PHARMACIST RECOMMENDED‡

NEW

MAXIMUM STRENGTH

Anti-Itch Cream

Pain Relieving Cream

  • Instantly soothes & relieves external itching & burning
  • Soothes irritated skin with aloe
  • Helps prevent further irritation
  • Fresh, clean scent

Compared to Vaglsil® Maximum Strength active ingredients‡‡

Relieves vaginal itching.

NDC 0363-0674-64

Well at Walgreens

WALGREENS PHARMACIST RECOMMENDED‡

MAXIMUM 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
637518benzocaine 20 % / resorcinol 3 % Vaginal CreamPSN1
637518benzocaine 200 MG/ML / resorcinol 30 MG/ML Vaginal CreamSCD1
637518benzocaine 20 % / resorcinol 3 % 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
47046-181-012022-01-28C16284748780-1d6a99b39-9a0e-a426-e053-dadaa90af4c2vaginal Anti-Itch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47046-181-01Well at Walgreens Anti-ItchMaximum Strength28 g in 1 TUBECREAM281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47046-181WELL AT WALGREENS ANTI-ITCH MAXIMUM STRENGTH (BENZOCAINE AND RESORCINOL) CREAM [ANICARE PHARMACEUTICALS PVT. LTD]1Legacy NDC, 1 package rows20201221_b6e209cb-9faa-4cb6-e053-2995a90a947a.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47046-18147046-181-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
b6e209cf-2a61-e7e3-e053-2a95a90a64dfb6e209cb-9faa-4cb6-e053-2995a90a947a2020-12-20WarningsExact identifier
spl id: b6e209cf-2a61-e7e3-e053-2a95a90a64df
spl set id: b6e209cb-9faa-4cb6-e053-2995a90a947a

Reported adverse events (FAERS/openFDA)#

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