FDA.reportPublic FDA data

CVS Anti-Itch Maximum Strength Cream

Manufacturer
CVS Health
Effective date
2024-11-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:36:50

Label at a glance#

ProductAnti-Itch Medicated Maximum Strength
Active ingredientBENZOCAINE, RESORCINOL
Label structure12 sections

Dosage and administration

Adults and children 12 years and older Apply a finger tip amount (approxiamtely a 1 inch strip) to the affected areas not more than 3 to 4 times daily Children under 12 years  ask a doctor

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

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

Allergy Allert

Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other –caine anesthetics.

Avoid contact with eyes

in case of contact rinse thoroughly and immediately with water.

Stop use and ask 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

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 12 years and older

Apply a finger tip amount (approxiamtely a 1 inch strip) to the affected areas not more than 3 to 4 times daily

Children under 12 years 

ask a doctor

Other Information:

OTHER SAFETY INFORMATION

questions?

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Mineral Oil, Cetyl Alcohol, Propylene Glycol, Glyceryl Stearate, PEG-100 Stearate, Isopropyl Palmitate, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Retinyl Palmitate, Zea Mays (Corn) Oil, Cholecalciferol, Lanolin Alcohol, Fragrance, Methylparaben, Carbomer, Isopropyl Myristate, Isopropyl Stearate, Sodium Sulfite, Triethanolamine, Trisodium EDTA, Maltodextrin

Principal Display Panel- Tube 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS          NDC 69842-588-28

Maximum StrengthAnti-Itch Creme

NET WT 1 oz. (28 g)

Principal Display Panel- TubePrincipal Display Panel- Tube

Principal Display Panel- TubePrincipal Display Panel- Tube

Principal Display Panel- Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS       69842-588-28

MAXIMUM STRENGTH ANTI ITCH CREAM 

NET WT 1.0 OZ (28g)

Principal Display Panel- CartonPrincipal Display Panel- Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
637518benzocaine 20 % / resorcinol 3 % Vaginal CreamPSN2
637518benzocaine 200 MG/ML / resorcinol 30 MG/ML Vaginal CreamSCD2
637518benzocaine 20 % / resorcinol 3 % 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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-588-28Anti-Itch Medicated Maximum Strength1 in 1 CARTONCREAM12
69842-588-28Anti-Itch Medicated Maximum Strength28 g in 1 TUBECREAM282

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-588ANTI-ITCH MEDICATED MAXIMUM STRENGTH (BENZOCAINE AND RESORCINOL) CREAM [CVS HEALTH]2Legacy NDC, 2 package rows20241114_69aa1822-c96b-46a0-95a6-7a7857331c69.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-58869842-588-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZOCAINEU3RSY48JW5ACTIB
RESORCINOLYUL4LO94HKACTIB
WATER059QF0KO0RIACT
MINERAL OILT5L8T28FGPIACT
CETYL ALCOHOL936JST6JCNIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
PEG-100 STEARATEYD01N1999RIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
CORN OIL8470G57WFMIACT
CHOLECALCIFEROL1C6V77QF41IACT
LANOLIN ALCOHOLS884C3FA9HEIACT
METHYLPARABENA2I8C7HI9TIACT
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)HHT01ZNK31IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ISOPROPYL STEARATE43253ZW1MZIACT
SODIUM SULFITEVTK01UQK3GIACT
TROLAMINE9O3K93S3TKIACT
TRISODIUM HEDTAK3E0U7O8KIIACT
MALTODEXTRIN7CVR7L4A2DIACT

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
e7848f0a-84e1-4f27-9bef-7ec2923c408369aa1822-c96b-46a0-95a6-7a7857331c692024-11-12WarningsExact identifier
spl id: e7848f0a-84e1-4f27-9bef-7ec2923c4083
spl set id: 69aa1822-c96b-46a0-95a6-7a7857331c69

Reported adverse events (FAERS/openFDA)#

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