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 27 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SPARTAN LIDOCAINE TIV PRIME SRL 4e04146a-ed19-2271-e063-6394a90a50f0 2026-03-27 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Lidocaine LIDOCAINE Walgreen Co. 41d5bdc4-66c8-31ab-e063-6394a90a1195 2026-03-27 Warnings Exact identifier application number: M017 Walgreens Cool N Heat Patch LIDOCAINE, MENTHOL Walgreen Co. 41d64a88-90fc-27ca-e063-6294a90a602b 2026-03-27 Warnings Exact identifier application number: M017 Softlips Naturals Medicated CAMPHOR, MENTHOL The Mentholatum Company 4e05d134-6c7f-1501-e063-6294a90ad27d 2026-03-27 Warnings Exact identifier application number: M017 Walgreens Cool N Heat Patch XL MENTHOL Walgreen Co. 41e92435-7f77-a593-e063-6394a90a4b38 2026-03-27 Warnings Exact identifier application number: M017 Walgreens Cool N Heat Back Patch MENTHOL Walgreen Co. 41e81110-4b79-1fa6-e063-6394a90ae90c 2026-03-27 Warnings Exact identifier application number: M017 Softlips Naturals Medicated Elderberry Acai CAMPHOR, MENTHOL The Mentholatum Company 4e0743a6-d450-043b-e063-6394a90ad1c2 2026-03-27 Warnings Exact identifier application number: M017 QFSN Pain Relief Cream PAIN RELIEF CREAM Qiaofusheng Pharmaceuticals Co., Ltd. 4d215da1-87f5-d35d-e063-6394a90ac348 2026-03-27 Warnings Exact identifier application number: M017 FlexSport Roll On METHYL SALICYLATE Pharmadel LLC bf8de3da-7628-6112-e053-2995a90a8e16 2026-03-26 Warnings Exact identifier application number: M017 Kofal Original METHYL SALICYLATE Pharmadel LLC 984780fd-496b-150b-e053-2995a90aed77 2026-03-26 Warnings Exact identifier application number: M017 Kofal Fuerte METHYL SALICYLATE Pharmadel LLC 98488a07-eba0-2b4e-e053-2995a90ad6ab 2026-03-26 Warnings Exact identifier application number: M017 Kofal Max Power MENTHOL Pharmadel LLC fe1f1408-b0cb-67a4-e053-6394a90ad609 2026-03-26 Warnings Exact identifier application number: M017 Kofal METHYL SALICYLATE Pharmadel LLC 9cac377d-97bc-f0b7-e053-2a95a90a2e12 2026-03-26 Warnings Exact identifier application number: M017 Milagroso CAMPHOR Pharmadel LLC 12b0401c-84d5-07cd-e063-6394a90a052c 2026-03-26 Warnings Exact identifier application number: M017 Ubredol METHYL SALICYLATE Pharmadel LLC fe96eead-1722-c05d-e053-6394a90a850f 2026-03-26 Warnings Exact identifier application number: M017 DZUL PAIN FREEZE INSTANT PAIN RELIEF MENTHOL Caball Sales, Inc. 4df3abcc-17f3-17f2-e063-6294a90afcca 2026-03-26 Warnings Exact identifier application number: M017 Equate Cool and Heat Extra Strength MENTHOL Wal-Mart Stores Inc ca3088a7-e1ec-4e69-80d9-fd0051bde938 2026-03-25 Warnings Exact identifier application number: M017 Ultra Strength Muscle Rub - CVS Health Ultra Strength Muscle Rub CAMPHOR, MENTHOL, METHYL SALICYLATE CVS Pharmacy 2ea95529-ec4b-c2ce-e063-6394a90a0739 2026-03-25 Warnings Exact identifier application number: M017 NUMBING CREAMS MENTHOL LIDOCAINE Yongchun Lihui Trading Co., Ltd. 4dd38cdf-d644-6da0-e063-6294a90afb3d 2026-03-25 Warnings Exact identifier application number: M017 ANTIPHLAMINE L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE Masaem Company 4dd3ab12-6cd3-1060-e063-6394a90a2dec 2026-03-25 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