Home NDC 67234-008 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 PRAMOXINE HYDROCHLORIDE; MENTHOL, UNSPECIFIED FORM
Active strength 10; 10 mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 67234-008 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 67234-008 67234-008-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 Ingredient Strength PRAMOXINE HYDROCHLORIDE 10 mg/g MENTHOL, UNSPECIFIED FORM 10 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 88AYB867L5 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1116155 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67234-008-01 Anti Itch Maximum Relief 42 g in 1 TUBE CREAM 42 4 67234-008-01 Anti Itch Maximum Relief 1 in 1 BOX CREAM 1 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67234-008 ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC] 3 Current NDC, Legacy NDC, 2 package rows 20250119_75de3d5e-ecbe-4d04-a39d-792200e6ee32.zip
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 108 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 67234-008-01 67234000801 1 TUBE in 1 BOX (67234-008-01) / 42 g in 1 TUBE 1 tube 2008-01-02 0000-00-00 No No Current