Home NDC 41520-295-16 Itch Relief
Product NDC 41520-295
Requested package NDC 41520-295-16
11-digit product format 415200295
Labeler code 41520
Product ID 41520-295_98de965d-ef3d-40cd-9686-fd83239e881c
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl, Zinc Acetate
Dosage form SPRAY
Route TOPICAL
Labeler American Sales Company
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2011-10-06
Marketing end 0000-00-00
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength 2 kg/100L; kg/100L
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record 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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2022-08-30 03:57 UTC · source 2022-08-29 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 I Inactivated by FDA bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DIPHENHYDRAMINE HYDROCHLORIDE ACTIVE INGREDIENT TC2D6JAD40 ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1 ZINC ACETATE ACTIVE INGREDIENT FM5526K07A ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1 DIPHENHYDRAMINE ACTIVE MOIETY 8GTS82S83M ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1 ZINC CATION ACTIVE MOIETY 13S1S8SF37 ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1 POVIDONE INACTIVE INGREDIENT FZ989GH94E ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1 TROMETHAMINE INACTIVE INGREDIENT 023C2WHX2V ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [AMERICAN SALES COMPANY] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 41520-295-16 41520029516 .059 L in 1 BOTTLE, SPRAY (41520-295-16) 2011-10-06 0000-00-00 No No Current