Home NDC 0363-4115 Walgreens Original Strength Anti Itch
Product NDC 0363-4115
11-digit product format 003634115
Labeler code 0363
Product ID 0363-4115_7c06a7e8-99c2-44e1-b47a-0da5d534ceab
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine hydrochloride, zinc acetate
Dosage form CREAM
Route TOPICAL
Labeler Walgreen Company
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-09-27
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength 1; .1 g/100g; g/100g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
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 Walgreens Original Strength Anti Itch
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 1 g/100g ZINC ACETATE .1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination TC2D6JAD40 Internal UNII lookup FM5526K07A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1292313 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0363-4115-28 Walgreens Original Strength Anti Itch 1 in 1 CARTON CREAM 1 12 0363-4115-28 Walgreens Original Strength Anti Itch 28 g in 1 TUBE CREAM 28 12
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DIPHENHYDRAMINE HYDROCHLORIDE ACTIVE INGREDIENT TC2D6JAD40 WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 ZINC ACETATE ACTIVE INGREDIENT FM5526K07A WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 DIPHENHYDRAMINE ACTIVE MOIETY 8GTS82S83M WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 ZINC CATION ACTIVE MOIETY 13S1S8SF37 WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 POLYOXYL 40 STEARATE INACTIVE INGREDIENT 13A4J4NH9I WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 STEARYL ALCOHOL INACTIVE INGREDIENT 2KR89I4H1Y WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1 WATER INACTIVE INGREDIENT 059QF0KO0R WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-4115 WALGREENS ORIGINAL STRENGTH ANTI ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [WALGREEN COMPANY] 11 Current NDC, Legacy NDC, 2 package rows 20231102_a6a49dbb-74c7-47ca-88f2-3bb3d9acf914.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 45 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join LUBRICAINE LIDOCAINE 4% ESBA LABORATORIES INC. 9d7416b1-607d-34e0-e053-2a95a90aa3c3 2026-01-08 Warnings Exact identifier application number: M017 0.5% LIDOCAINE BURN RELIEF LIDOCAINE HYDROCHLORIDE Universal Distribution Center LLC 0a1aeff0-bade-457b-a0ac-099d646c0b2e 2026-01-08 Warnings Exact identifier application number: M017 4% MENTHOL COLD THERAPY MENTHOL Universal Distribution Center LLC 66892993-a755-4584-b2a8-2e8d7ac70593 2026-01-08 Warnings Exact identifier application number: M017 Private Label Antifungal Barrier Cream 2% MICONAZOLE NITRATE CREAM Swiss-American CDMO, LLC e74bddea-c1ac-4e4e-84bd-5a9defb85b2d 2026-01-08 Warnings Exact identifier application number: M017 2.0% LIDOCAINE BURN LIDOCAINE HYDROCHLORIDE Universal Distribution Center LLC e1911279-85f7-4053-b6da-8f4e991347a2 2026-01-08 Warnings Exact identifier application number: M017 POMG PAIN RELIEF ROLLER LIDOCAINE HYDROCHLORIDE, MENTHOL POMG LLC 1fa980fb-fc0e-fdd0-e063-6394a90adc13 2026-01-07 Warnings Exact identifier application number: M017 Artridon Glucosamine MENTHOL, METHYL SALICYLATE Pharmadel LLC 73572156-4cce-0669-e053-2991aa0aaecc 2026-01-07 Warnings Exact identifier application number: M017 HealthWise Cooling Pain Relief MENTHOL Veridian Healthcare 6e2ad0ab-e3a8-4e3a-8f1d-2cd6351185bd 2026-01-07 Warnings Exact identifier application number: M017 Hydrocortisone 1% Anti-Itch Cream HYDROCORTISONE DLC Laboratories, Inc. 16eeec2c-065d-4da0-e063-6294a90a3873 2026-01-07 Warnings Exact identifier application number: M017 Maximum Strength Hydrocortisone HYDROCORTISONE DLC Laboratories, Inc caf50f12-f35c-4e9e-8ef7-3b0c84e225ee 2026-01-07 Warnings Exact identifier application number: M017 EARTHS CARE MUSCLE AND JOINT RUB CAMPHOR DLC Laboratories, Inc. 71e33e06-4dc3-4ead-a122-ff89d93a64de 2026-01-07 Warnings Exact identifier application number: M017 Amour CBD PAIN RELIEF CREAM SVD Premium Products 95b45e79-b1e7-17b2-e053-2995a90a8836 2026-01-07 Warnings Exact identifier application number: M017 Tiger Balm Active Muscle METHYL SALICYLATE AND MENTHOL, UNSPECIFIED FORM Haw Par Healthcare Ltd. 845a4ead-f9c0-4009-bcae-b17cd388439b 2026-01-07 Warnings Exact identifier application number: M017 3X Medicated Toothache and Gum Gel BENZOCAINE Rite Aid 996f7989-17ce-5b28-e053-2995a90af8b8 2026-01-06 Warnings Exact identifier application number: M017 QNTAMAX Muscle and Joint Pain Relieving CAMPHOR (SYNTHETIC), MENTHOL Qntamax LLC 6622b94c-824e-4e84-a8d8-b60bb0b866e2 2026-01-06 Warnings Exact identifier application number: M017 Winco Muscle and Joint Pain Relief Gel 2oz WINCO BENGAY VANISHING SCENT MUSCLE AND JOINT PAIN RELIEF WINCO FOODS, LLC 47bedf4e-4036-cf43-e063-6394a90a91d6 2026-01-06 Warnings Exact identifier application number: M017 Pain Relief Hot Patch MENTHOL AND CAPSAICIN Universal Distribution Center LLC 110bcb16-ef0b-4bc8-8877-173a0494e1ad 2026-01-06 Warnings Exact identifier application number: M017 WOFANLI Quit Smoking Nicotine Patches NICOTINE PATCHES Shenzhen Paxi Trading Co., Ltd. 4582b4e9-0c24-069d-e063-6394a90a6f4b 2026-01-05 Warnings Exact identifier application number: M017 Lidocaine 4% Topical Anesthetic Cream LIDOCAINE 4% Oncor Pharmaceuticals 1baaa669-05af-4024-a0ba-ee3451756f6a 2026-01-05 Warnings Exact identifier application number: M017 TheraCare Pain Relief MENTHOL Veridian Healthcare 6834a6de-4d1d-4e40-945d-ec5c267abd14 2026-01-05 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 0363-4115-28 00363411528 1 TUBE in 1 CARTON (0363-4115-28) / 28 g in 1 TUBE 1 tube 2013-09-27 0000-00-00 No No Current