Eurax

Product NDC
69489-311
11-digit product format
694890311
Labeler code
69489
Product ID
69489-311_4640ba32-cf20-18ad-e063-6394a90a4592
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
crotamiton
Dosage form
CREAM
Route
TOPICAL
Labeler
Journey Medical Corporation
Application
NDA006927
Marketing category
NDA
Marketing start
2026-03-16
Substance
CROTAMITON
Active strength
100 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Eurax
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CROTAMITON100 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiD6S4O4XD0H
Rxcui207864, 309552

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2ea7942c-f3b4-4c60-49a3-bfc71c3c134eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69489-311-60Eurax60 g in 1 TUBECREAM602
69489-311-60Eurax1 in 1 CARTONCREAM12

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
309552crotamiton 10 % Topical CreamPSN99c826aa-c7dd-4e60-be9c-e9c151033d132
207864Eurax 10 % Topical CreamPSN99c826aa-c7dd-4e60-be9c-e9c151033d132
207864crotamiton 100 MG/ML Topical Cream [Eurax]SBD99c826aa-c7dd-4e60-be9c-e9c151033d132
309552crotamiton 100 MG/ML Topical CreamSCD99c826aa-c7dd-4e60-be9c-e9c151033d132
309552crotamiton 10 % Topical CreamSY99c826aa-c7dd-4e60-be9c-e9c151033d132
207864Eurax 10 % Topical CreamSY99c826aa-c7dd-4e60-be9c-e9c151033d132

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69489-311-60694890311601 TUBE in 1 CARTON (69489-311-60) / 60 g in 1 TUBE1 tube2026-03-16NoNoHistorical