Anti Itch

Product NDC
67234-008
11-digit product format
672340008
Labeler code
67234
Product ID
67234-008_eba79205-9b9e-495e-a57c-c1d980a90e22
Type
HUMAN OTC DRUG
Nonproprietary name
Pramoxine Hydrochloride and Menthol
Dosage form
CREAM
Route
TOPICAL
Labeler
Natureplex LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2008-01-02
Substance
MENTHOL, UNSPECIFIED FORM; PRAMOXINE HYDROCHLORIDE
Active strength
10; 10 mg/g; mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Anti Itch Maximum ReliefPRAMOXINE HYDROCHLORIDE AND MENTHOLNatureplex LLC75de3d5e-ecbe-4d04-a39d-792200e6ee322025-08-28WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warnings For external use only. Avoid contact with eyes and nose. Not for prolonged use. Do not use on large areas of the body Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days redness, irritation, swelling, or pain develops, persists, or increases If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Additional Listing Data#

Finished product
Yes
Brand name base
Anti Itch
Brand name suffix
Maximum Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PRAMOXINE HYDROCHLORIDE10 mg/g
MENTHOL, UNSPECIFIED FORM10 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii88AYB867L5, L7T10EIP3A
Rxcui1116155

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67234-008-01Anti Itch Maximum Relief42 g in 1 TUBECREAM424
67234-008-01Anti Itch Maximum Relief1 in 1 BOXCREAM14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MentholACTIVE INGREDIENTL7T10EIP3AANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
Pramoxine HydrochlorideACTIVE INGREDIENT88AYB867L5ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
MentholACTIVE MOIETYL7T10EIP3AANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
PramoxineACTIVE MOIETY068X84E056ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)INACTIVE INGREDIENT4Q93RCW27EANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
CETOSTEARYL ALCOHOLINACTIVE INGREDIENT2DMT128M1SANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
DMDM HYDANTOININACTIVE INGREDIENTBYR0546TOWANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
POLYSORBATE 60INACTIVE INGREDIENTCAL22UVI4MANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
TROLAMINEINACTIVE INGREDIENT9O3K93S3TKANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1
WATERINACTIVE INGREDIENT059QF0KO0RANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67234-008ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]3Current NDC, Legacy NDC, 2 package rows20250119_75de3d5e-ecbe-4d04-a39d-792200e6ee32.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1116155menthol 1 % / pramoxine HCl 1 % Topical CreamPSN75de3d5e-ecbe-4d04-a39d-792200e6ee324
1116155menthol 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical CreamSCD75de3d5e-ecbe-4d04-a39d-792200e6ee324
1116155menthol 1 % / pramoxine hydrochloride 1 % Topical CreamSY75de3d5e-ecbe-4d04-a39d-792200e6ee324

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67234-008-01672340008011 TUBE in 1 BOX (67234-008-01) / 42 g in 1 TUBE1 tube2008-01-020000-00-00NoNoCurrent