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 2 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join ActivICE MENTHOL Medline Industries, LP 834adeb9-38ad-0cfe-e053-2991aa0af82f 2026-09-01 Warnings Exact identifier application number: M017 La Vaquita New Extra METHYL SALICYLATE, MENTHOL Delon Laboratories (1990) Ltd 3097a01b-cee5-492f-b65a-63992fb28e3a 2026-09-01 Warnings Exact identifier application number: M017 Terramed Just Think Comfort Hydrocortisone 1% Cream HYDROCORTISONE Rida LLC 0d2c0c2c-370f-4adb-b0ea-1e218c927f8b 2026-09-01 Warnings Exact identifier application number: M017 Itch Stopping DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE HyVee Inc 53157137-b980-45d2-aa10-8c111c0ec2f4 2026-08-31 Warnings Exact identifier application number: M017 ndc (product): 42507-622 EAYONYUMT NECK PAIN RELIEF MENTHOL Wuhan Ruihengjie Technology Co., Ltd. 5a450e68-07a7-a4bb-e063-6294a90a97c9 2026-08-30 Warnings Exact identifier application number: M017 EAYONYUM BACK PAIN RELIEVING MENTHOL Wuhan Ruihengjie Technology Co., Ltd. 5a458280-4f9c-5af6-e063-6394a90acb2e 2026-08-30 Warnings Exact identifier application number: M017 EAYONYUM KNEE PAIN RELIEVING MENTHOL Wuhan Ruihengjie Technology Co., Ltd. 5a45d19f-c753-71eb-e063-6294a90a4805 2026-08-30 Warnings Exact identifier application number: M017 Good Neighbor Pharmacy Hydrocortisone With Aloe for Sensitive Skin HYDROCORTISONE AmerisourceBergen c5c5b5ca-b4d4-4fa8-b647-b3ccb2966495 2026-08-30 Warnings Exact identifier application number: M017 Olu Pain Management LIDOCAINE AND CAMPHOR HAWAII REPACK, INC. 31ed3d82-ba12-46b2-b0ec-7e5e019efc10 2026-08-28 Warnings Exact identifier application number: M017 4% Lidocaine Patches 4% LIDOCAINE PATCHES Shenzhen Chaoxiji Technology Co.,Ltd. 5a177987-7c05-f07f-e063-6394a90aa9ba 2026-08-28 Warnings Exact identifier application number: M017 Relieved Pro Wrap 4% LIDOCAINE PATCH Transfer Technology 5a1c6ebf-ad3f-c47b-e063-6294a90aa19a 2026-08-28 Warnings Exact identifier application number: M017 Sinsinpas Arex Pain Relieving Patch, Medium CAMPHOR, MENTHOL, METHYL SALICYLATE Sinsin Pharmaceutical Co., Ltd. 46453ef2-512b-4852-e063-6394a90a8912 2026-08-28 Warnings Exact identifier application number: M017 Sinsinpas arex patch large CAMPHOR, MENTHOL, METHYL SALICYLATE Sinsin Pharmaceutical Co., Ltd. 47c242da-56cd-bea1-e063-6394a90a41de 2026-08-28 Warnings Exact identifier application number: M017 4% Lidocaine Patches 4% LIDOCAINE PATCHES Shenzhen Chaoxiji Technology Co.,Ltd. 5a16c6aa-3ab0-3e46-e063-6294a90a6d8f 2026-08-27 Warnings Exact identifier application number: M017 Lidocaine Patch 4% LIDOCAINE 4% Global America Group LLC 1eec782d-0e56-43d2-b842-da0ae47c5dc9 2026-08-26 Warnings Exact identifier application number: M017 Careland Lidocaine Plus Menthol Pain Relieving LIDOCAINE, MENTHOL Planet (Anhui) Pharmaceutical Co., Ltd 0f928b5b-60f5-4a45-a409-c601eb330487 2026-08-26 Warnings Exact identifier application number: M017 PARCHE CALIENTE CAPSAICINA AND MENTOL DW SUPPORT LLC 59f2708e-295a-ccb3-e063-6394a90ad395 2026-08-26 Warnings Exact identifier application number: M017 CVS Pain Relief LIDOCAINE CVS Pharmacy 4ecbc263-e0d4-18d5-e063-6294a90a72e9 2026-08-26 Warnings Exact identifier application number: M017 CVS Pain Relief Lidocaine XL LIDOCAINE CVS Pharmacy 4aa286e3-e274-8095-e063-6394a90ae871 2026-08-26 Warnings Exact identifier application number: M017 TERAPIA DE DIA Y NOCHE PAIN RELIEVING PATCH DW SUPPORT LLC 59f44135-865b-9d7d-e063-6294a90a9dd9 2026-08-26 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