Home NDC 42507-622 Itch Stopping
Product NDC 42507-622
11-digit product format 425070622
Labeler code 42507
Product ID 42507-622_7a9541e1-5f0c-4547-81bd-647e1344bf12
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine Hydrochloride, Zinc Acetate
Dosage form CREAM
Route TOPICAL
Labeler HyVee Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-09-27
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength 2; .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 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 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 42507-622-64 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 42507-622-64 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 42507-622-64 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 42507-622-64 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 42507-622-64 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 42507-622-64 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 42507-622-64 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 42507-622-64 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 42507-622-64 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 42507-622-64 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 42507-622-64 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 42507-622-64 557ba5c1ecfa…9c80585c8c6e…
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 Itch Stopping
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 2 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 1087026 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DIPHENHYDRAMINE HYDROCHLORIDE ACTIVE INGREDIENT TC2D6JAD40 ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 ZINC ACETATE ACTIVE INGREDIENT FM5526K07A ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 DIPHENHYDRAMINE ACTIVE MOIETY 8GTS82S83M ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 ZINC CATION ACTIVE MOIETY 13S1S8SF37 ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 CETYL ALCOHOL INACTIVE INGREDIENT 936JST6JCN ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 DIAZOLIDINYL UREA INACTIVE INGREDIENT H5RIZ3MPW4 ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 PEG-2 STEARATE INACTIVE INGREDIENT 94YQ11Y95F ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 PEG-20 STEARATE INACTIVE INGREDIENT NBX892EA57 ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [HYVEE INC] 1
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 143 of 151 · 3,010 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join PURE EASE Joint Muscle lnstant Pain Relief CAPSAICIN, MENTHOL SERENU, INC. 42bf129c-5c84-4331-b6d0-78e3be71a985 2023-11-13 Warnings Exact identifier application number: M017 PURE EASE Neur Cream Instant Deep Pain Relief CAPSAICIN, MENTHOL SERENU, INC. e46a4636-6405-440a-a05a-862c354bab54 2023-11-13 Warnings Exact identifier application number: M017 Cryomax Cooling MENTHOL LIFE WEAR TECHNOLOGIES 0a0ae5ba-9fac-45f6-e063-6294a90ad555 2023-11-13 Warnings Exact identifier application number: M017 LBri Super Aloe Stop The Pain METHYL SALICYLATE, MENTHOL, CAPSAICIN L'Bris, Pure 'N Natural 8fb2010c-c34b-4552-858d-a0188ad313ad 2023-11-11 Warnings Exact identifier application number: M017 TOTAL RELIEF HYDROCORTISONE DR. MARDER SKINCARE, LLC 2c05459c-5a2c-45ab-b534-87f966b41681 2023-11-11 Warnings Exact identifier application number: M017 Human Science Muscle Pain Relief METHYL SALICYLATE, MENTHOL Human Science, LLC 4bccc017-264b-11ce-e054-00144ff8d46c 2023-11-11 Warnings Exact identifier application number: M017 Lidozen LIDOCAINE HYDROCHLORIDE, MENTHOL Village Pharma, LLC 55108ffd-d6a8-41de-e054-00144ff88e88 2023-11-11 Warnings Exact identifier application number: M017 Debbies Down and Dirty Deep Tissue Joint and Muscle MENTHOL DD&D Manufacturing Co., Ltd 531fe834-53e3-305f-e054-00144ff88e88 2023-11-11 Warnings Exact identifier application number: M017 TerraFreeze Pain Relief MENTHOL,METHYL SALICYLATE,HISTAMINE DIHYDROCHLORIDE Beyond Derma, LLC 81dc70b3-7e93-4f9a-ae3a-b50bbfd1a677 2023-11-11 Warnings Exact identifier application number: M017 GOLD ICE Pain Relief MENTHOL Eden's Answers, Inc. a1356c39-42b9-4bd8-a873-bcd40717058b 2023-11-11 Warnings Exact identifier application number: M017 RUBBING DOTS NATURAL COOL PAIN RELIEF MENTHOL Awesome Trading, LLC 137a88ff-e409-4a67-addc-883194c356ae 2023-11-11 Warnings Exact identifier application number: M017 MAXOCAINE Lidocaine Hemp Oil Topical Analgesic LIDOCAINE HYDROCHLORIDE Prime Commerce, LLC 28ed2149-38d2-4062-8442-990a98a69cfc 2023-11-11 Warnings Exact identifier application number: M017 MAXOCAINE PAIN RELIEVING ROLL-ON LIDOCAINE HYDROCHLORIDE, MENTHOL Prime Commerce, LLC c263d5f2-89b9-4dfd-91c8-f894e5f956c9 2023-11-11 Warnings Exact identifier application number: M017 SUGAR BRANDS Rescue Pain Relief and Recovery LIDOCAINE HYDROCHLORIDE Sugar Brands, LLC 74013709-d1d5-4425-825d-eee726718c61 2023-11-11 Warnings Exact identifier application number: M017 NATURES CRAFT LIDOCAINE Male Genital Desensitizer LIDOCAINE HYDROCHLORIDE Natures Design Products LLC 61bf1776-5c6c-4307-8348-41fa60164017 2023-11-11 Warnings Exact identifier application number: M017 CLEAN REMEDIES CR PAIN RELIEF MENTHOL Clean Remedies, LLC aea9291d-3244-401c-9607-e91107228faa 2023-11-11 Warnings Exact identifier application number: M017 Arth Arrest METHYL NICOTINATE, CAPSAICIN Key 2 Health, Inc. 495034ac-dbf5-4c55-906b-6ffcbcfd5bc2 2023-11-11 Warnings Exact identifier application number: M017 KINETIC ICE Muscle and Joint Pain Relief Cream MENTHOL No Reason, LLC 565f0e20-e534-41db-ba20-e726d578405f 2023-11-11 Warnings Exact identifier application number: M017 KARMA RUB Elemental Pain Relief LIDOCAINE HYDROCHLORIDE Elemental Bliss LLC c224fb1b-827f-461e-a58f-4020700c3e0d 2023-11-11 Warnings Exact identifier application number: M017 Bakers Best Arthritis Pain Relief with Hemp Seed HISTAMINE DIHYDROCHLORIDE Baker's Best Health Products, LLC 46415d28-99b5-4c9e-bde9-1c703595f671 2023-11-11 Warnings Exact identifier application number: M017
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 42507-622-64 42507062264 1 TUBE in 1 CARTON (42507-622-64) / 28 g in 1 TUBE (42507-622-28) 1 tube 2015-09-27 No No Current