Home NDC 0363-0263 Walgreen Anti-Itch
Product NDC 0363-0263
11-digit product format 003630263
Labeler code 0363
Product ID 0363-0263_43fa8f25-5892-cf6f-e063-6294a90a92db
Type HUMAN OTC DRUG
Nonproprietary name Pramoxine HCL
Dosage form LOTION
Route TOPICAL
Labeler Walgreens
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-08
Substance PRAMOXINE HYDROCHLORIDE
Active strength 1 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 Walgreen Anti-Itch
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PRAMOXINE HYDROCHLORIDE 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 88AYB867L5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1246075 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 0363-0263-75 Walgreen Anti-Itch 212 g in 1 BOTTLE, PUMP LOTION 212 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-0263 WALGREEN ANTI-ITCH (PRAMOXINE HCL) LOTION [WALGREENS] 2 Current NDC, Legacy NDC, 1 package rows 20231212_b5f9d1c5-891e-4377-e053-2995a90aa281.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 61 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Nighttime 4X Medicated Cream BENZOCAINE Rite Aid 21645ed1-2dc0-223a-e063-6394a90ab021 2025-11-21 Warnings Exact identifier application number: M017 4x Medicated Gum Cream BENZOCAINE Albertsons b81a308c-9c30-0e3d-e053-2a95a90a15d2 2025-11-21 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC b0edd9d9-951f-d3dd-e053-2995a90a8d5a 2025-11-21 Warnings Exact identifier application number: M017 Up up LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES Target Corporation 44121d40-86e1-0df6-e063-6294a90aedaf 2025-11-20 Warnings Exact identifier application number: M017 Up up PAIN RELIEF ADVANCED HYDROGEL PATCHES Target Corporation 44128b70-3172-ee37-e063-6294a90a705f 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC f03090fa-f7e6-f53a-e053-2a95a90aa819 2025-11-20 Warnings Exact identifier application number: M017 HEATING PAIN RELIEF METHYL SALICYLATE, MENTHOL SUNSET NOVELTIES, INC ff073e47-3107-e17e-e053-6294a90a58fa 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC fc8a8f20-97ab-481e-e053-6394a90a3525 2025-11-20 Warnings Exact identifier application number: M017 MENTHOL MENTHOL SUNSET PAIN RELIEF ROLL-ON 3OZ 934d4638-b47b-187d-e053-2995a90ae69d 2025-11-20 Warnings Exact identifier application number: M017 FOOT PAIN RELIEF ROLL-ON LIDOCAINE, MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 43edcea0-ab04-f368-e063-6294a90a817a 2025-11-19 Warnings Exact identifier application number: M017 Absolut Skin Corticosoothe Anti-Itch HYDROCORTISONE Absolut Skin Incorporated deb52218-9176-4aaa-a22f-b66dada6690f 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy LIDOCAINE InterMed Laboratories Private Limited 43f3d189-f6b7-02ed-e063-6394a90afd73 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch HealthA2Z LIDOCAINE InterMed Laboratories Private Limited 43f3e288-e828-8130-e063-6394a90a6d44 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Leader LIDOCAINE InterMed Laboratories Private Limited 42f06914-c8b8-ea9c-e063-6294a90a79e6 2025-11-19 Warnings Exact identifier application number: M017 CVS Anti-Itch CAMPHOR, MENTHOL CVS 87715662-c788-9a8d-e053-2a95a90acb53 2025-11-19 Warnings Exact identifier application number: M017 Walgreen Anti Itch CAMPHOR, MENTHOL Walgreens b4f47a8d-d4a6-9233-e053-2a95a90afd90 2025-11-19 Warnings Exact identifier application number: M017 Leader Anti-Itch CAMPHOR, MENTHOL LEADER/Cardinal Helath 110, Inc. 9ca985c6-5017-0558-e053-2995a90a8202 2025-11-19 Warnings Exact identifier application number: M017 CVS Anti-Itch PRAMOXINE HCL CVS 87fc476a-5b12-7383-e053-2995a90a530b 2025-11-19 Warnings Exact identifier application number: M017 Walgreen Anti-Itch PRAMOXINE HCL Walgreens b5f9d1c5-891e-4377-e053-2995a90aa281 2025-11-19 Warnings Exact identifier application number: M017 ndc (product): 0363-0263 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET PAIN RELIEF 89f5f688-856f-f2df-e053-2995a90a73cf 2025-11-19 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 0363-0263-75 00363026375 212 g in 1 BOTTLE, PUMP (0363-0263-75) 212 g 2020-12-08 0000-00-00 No No Current