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 33 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tylenol Precise Cooling Pain Relieving LIDOCAINE, MENTHOL Kenvue Brands LLC fc0a3404-b174-3952-e053-6294a90a1e02 2026-02-16 Warnings Exact identifier application number: M017 Aloe Vera Gel LIDOCAINE HCL Valu Merchandisers Company 87ee2b4f-d640-4cec-9f48-1d8aa54434e9 2026-02-16 Warnings, Adverse reactions Exact identifier application number: M017 Hemp Magic Fast-Acting Pain Relief Cream MENTHOL Nexxus Capital LLC 4af69640-1413-868b-e063-6394a90a3989 2026-02-16 Warnings Exact identifier application number: M017 RelaxInk LIDOCAINE LIDOCAINE 4% Hambli Limited 49a1cf66-9bb1-b918-e063-6394a90a2ff6 2026-02-15 Warnings Exact identifier application number: M017 blue goo Pain Relieving MENTHOL 2.5% Garcoa, Inc. 7b9b5ac6-9568-464c-8096-0302a1e650df 2026-02-13 Warnings Exact identifier application number: M017 Methyl Salicylate 30 Percent Cream METHYL SALICYLATE Alexso, Inc 1d50ccb2-1a5d-49c7-8524-2f54eed63e85 2026-02-13 Warnings Exact identifier application number: M017 Antiseptic Mouth Rinse EUCALYPTOL, MENTHOL, METHYOL SALICYLATE, THYMOL Topco Associates LLC a38e91c1-7ac6-4a7f-a5a2-8d9166b1535a 2026-02-13 Warnings, Adverse reactions Exact identifier application number: M017 Gel Cooling Pain Relief MENTHOL Topco Associates LLC 80962394-a46f-48fd-8e0c-685dd1e500d7 2026-02-13 Warnings, Adverse reactions Exact identifier application number: M017 Banophen DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE Major Pharmaceuticals 9758d886-bd58-4eb2-a827-fa8e7fee2b7c 2026-02-13 Warnings Exact identifier application number: M017 Natureplex Hydrocortisone Hydro HYDROCORTISONE Natureplex, LLC 2fc6a148-34bb-4289-8588-32c1bb011b98 2026-02-13 Warnings Exact identifier application number: M017 Capsaicin 0.035 Percent CAPSAICIN Alexso, Inc 6d0bc1cc-e812-4753-b20c-c0357dd6deb5 2026-02-13 Warnings Exact identifier application number: M017 Swiftalyn Numbing Cream LIDOCAINE 4% GENUINE INNOVATION LTD 3f74c4a6-26f0-ddf7-e063-6394a90a1225 2026-02-12 Warnings Exact identifier application number: M017 PHARMBANNER Arnica Bruise Cream ARNICA BRUISE CREAM Shenzhen Xinxin Yunhai Technology Co., Ltd. 3c783061-8e2d-8a84-e063-6394a90a5265 2026-02-12 Warnings Exact identifier application number: M017 ETERNAL SPIRIT BEAUTY PAIN RELIEF WITH HEMP MENTHOL, CAMPHOR Worldwide Cosmetics, Inc 459d64a9-0538-57c8-e063-6394a90a6155 2026-02-12 Warnings Exact identifier application number: M017 Antiseptic Mouth Rinse EUCALYPTOL Walgreen Co. cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0 2026-02-12 Warnings, Adverse reactions Exact identifier application number: M017 Medicated Body Powder MENTHOL Walmart Stores Inc afd337b7-d76e-f17a-e053-2a95a90abac7 2026-02-12 Warnings Exact identifier application number: M017 Lidocaine Hydrochloride 2% LIDOCAINE HYDROCHLORIDE Aldermed Inc. 4977b722-d08d-3d9e-e063-6294a90a9035 2026-02-12 Warnings Exact identifier application number: M017 Ice Gel ICE COLD ANALGESIC MENTHOL Jell Pharmaceuticals Pvt Ltd 4a8b3f84-8c45-eb94-e063-6394a90a3e73 2026-02-11 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Lidocaine Patch LIDOCAINE Walgreen Co. 41c4e9fe-e407-b22a-e063-6394a90a4b27 2026-02-10 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE CREAM 1% Aldermed Inc. 4a7f2c0e-5cf3-29cb-e063-6394a90a5d8d 2026-02-10 Warnings Exact identifier application number: M017
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