Home NDC 37808-622 itch relief
Product NDC 37808-622
11-digit product format 378080622
Labeler code 37808
Product ID 37808-622_73bec294-055a-4342-9cdf-00cd83e1d0ad
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine Hydrochloride, Zinc Acetate
Dosage form CREAM
Route TOPICAL
Labeler H E B
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-09-15
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 2026-12-31
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2019-12-08 06:16 UTC · source 2019-12-05 excluded product product 37808-622 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 37808-622 37808-622-64 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…
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 relief
Listing expiration 2026-12-31 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-622-64 itch relief 1 in 1 CARTON CREAM 1 3 37808-622-64 itch relief 28 g in 1 TUBE CREAM 28 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DIPHENHYDRAMINE HYDROCHLORIDE ACTIVE INGREDIENT TC2D6JAD40 ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 ZINC ACETATE ACTIVE INGREDIENT FM5526K07A ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 DIPHENHYDRAMINE ACTIVE MOIETY 8GTS82S83M ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 ZINC ACTIVE MOIETY J41CSQ7QDS ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 CETYL ALCOHOL INACTIVE INGREDIENT 936JST6JCN ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 DIAZOLIDINYL UREA INACTIVE INGREDIENT H5RIZ3MPW4 ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-622 ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B] 3 Current NDC, Legacy NDC, 2 package rows 20241015_34c7bcd3-203f-4630-894d-3739a1576c8d.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 52 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Large Medicate Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Amerisource Bergen a7d5f89b-59b9-4603-99aa-273b85be813e 2025-12-22 Warnings Exact identifier application number: M017 Good Neighbor Capsaicin Heat Patch for Back CAPSAICIN Amerisource Bergen f873a0b8-8123-1600-e053-6394a90a043e 2025-12-22 Warnings Exact identifier application number: M017 Good Neighbor Pharmacy Cold Therapy Pain Relief Patch MENTHOL Amerisource Bergen f872f371-b92c-f5d5-e053-6294a90a7dcd 2025-12-22 Warnings Exact identifier application number: M017 Caring Mills Hydrocortisone HYDROCORTISONE Veridian Healthcare b0b1889b-3099-4943-a4cb-d9a898a06860 2025-12-22 Warnings Exact identifier application number: M017 LIDOCAINE 5% LIDOCAINE Medhome Pharma Inc 46968f5a-d214-9871-e063-6394a90ab45d 2025-12-22 Warnings Exact identifier application number: M017 Blue-Emu THRIVE Cooling TRIPELENNAMINE 0.5% Kingsway Pharmaceuticals dba NFI, LLC 7ac6456a-42c5-4ac8-aae6-db4abfda9df0 2025-12-22 Warnings Exact identifier application number: M017 MENTHOL MENTHOL SUNSET PAIN RELIEF 45c5ca6f-d425-6cfb-e063-6394a90a1b66 2025-12-20 Warnings Exact identifier application number: M017 HERSTAT GST Genital Sore Treatment CAMPHOR, MENTHOL Herstat (USA) Inc. e8d27684-fb15-2e6a-e053-2a95a90a248f 2025-12-19 Warnings Exact identifier application number: M017 Kroger Anti Itch HYDROCORTISONE The Kroger Co 46547277-f11a-b9e7-e063-6294a90a2ccd 2025-12-19 Warnings Exact identifier application number: M017 Kroger Cool and Heat Roll-On MENTHOL Kroger 46551d07-3006-c3ec-e063-6294a90aa3f2 2025-12-19 Warnings Exact identifier application number: M017 Naughty Kitty Kat NO GAG DEEP THROAT SPRAY INKED SUGAR, INC 170eb644-c72c-5744-e063-6394a90a767d 2025-12-19 Warnings Exact identifier application number: M017 Tiger Balm Red Extra Strength CAMPHOR (SYNTHETIC) AND MENTHOL Haw Par Healthcare Ltd. ce703715-4c11-472c-9270-daac87b7be05 2025-12-19 Warnings Exact identifier application number: M017 Aspercreme with Lidocaine Foot Pain Creme LIDOCAINE HYDROCHLORIDE Chattem, Inc. da82cc0e-cc39-408e-87e1-c35bb6f9f51e 2025-12-19 Warnings Exact identifier application number: M017 Health Trak Plus Menthol-Infused Pain Relief Socks MENTHOL Railroad Sock LLC 43413e55-1db2-fc1a-e063-6394a90a7167 2025-12-18 Warnings Exact identifier application number: M017 BIO-ICE MENTHOL, CAMPHOR Electrostim Medical Services Inc. d/b/a EMSI 1bfd1468-9139-43b1-9709-d47b63d17cfb 2025-12-18 Warnings Exact identifier application number: M017 Lidotrode LIDOCAINE Strand Health Group 1fd20b9a-b8bc-c94f-e063-6394a90a2b69 2025-12-18 Warnings Exact identifier application number: M017 A Health Itch Relief Gel ITCH RELIEF GEL Bionpharma, Inc. ecf5decb-c98b-7739-e053-2995a90a5541 2025-12-18 Warnings Exact identifier application number: M017 After Burn 2.5% LIDOCAINE HCL Tender Corporation d/b/a Adventure Ready Brands 4640395f-a76c-d022-e063-6294a90adde6 2025-12-18 Warnings Exact identifier application number: M017 SPARTAN WIPES ENDURANCE WIPES TIV PRIME SRL 26d02431-2c95-001c-e063-6394a90a29c7 2025-12-18 Warnings Exact identifier application number: M017 Stopain Extra Strength Continuous MENTHOL Troy Manufacturing, Inc. a0f76968-d22c-4b1c-a9e6-8d0179a2e98e 2025-12-18 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 37808-622-64 37808062264 1 TUBE in 1 CARTON (37808-622-64) / 28 g in 1 TUBE 1 tube 2010-09-15 0000-00-00 No No Current