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 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 · 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 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 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 92 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Bliss Republic Lidocaine Numbing Cream LIDOCAINE NUMBING CREAM Sargass Group Limited Liability Company 35415851-beba-5bb4-e063-6294a90a35c0 2025-05-16 Warnings Exact identifier application number: M017 Cold Hot Chinese Red Tiger Pain Relief Gel Roll-On MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 352798e1-1e09-3d47-e063-6394a90ad404 2025-05-15 Warnings Exact identifier application number: M017 Plantar Fasciitis Chinese Red Tiger Pain Relief Gel Roll-On MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 35285d62-c660-a056-e063-6294a90aabc8 2025-05-15 Warnings Exact identifier application number: M017 SionBiotext Hydrocortisone HYDROCORTISONE ACETATE 1% Sion Biotext Medical Ltd 35073eae-26fe-2bb5-e063-6294a90ab56a 2025-05-13 Warnings Exact identifier application number: M017 Bliss Republic Lidocaine Numbing Cream LIDOCAINE NUMBING CREAM Sargass Group Limited Liability Company 3508ae14-d9c9-3c85-e063-6294a90a0098 2025-05-13 Warnings Exact identifier application number: M017 SORE NO MORE WARM THERAPY MENTHOL AND CAMPHOR SOMBRA COSMETICS INC. cd86b56e-9b4c-4aca-9740-c8793cb12055 2025-05-12 Warnings Exact identifier application number: M017 SORE NO MORE COOL THERAPY MENTHOL SOMBRA COSMETICS INC. 9aa1f0ac-3baf-4e45-9e3a-c28a99b22909 2025-05-12 Warnings Exact identifier application number: M017 Calm and Correct Serum with Lidocaine LIDOCAINE 3 PERCENT Renu Laboratories, LLC ddcf1c2e-2f67-44d7-e053-2a95a90a812b 2025-05-09 Warnings Exact identifier application number: M017 Mqupin Knee Patch KNEE PATCH Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd 09772e4b-8193-3771-e063-6394a90a9516 2025-05-08 Warnings Exact identifier application number: M017 Hydrocortisone Cream HYDROCORTISONE Trifecta Pharmaceuticals USA d57a59fb-c8f2-f73b-e053-2995a90a4cdb 2025-05-08 Warnings Exact identifier application number: M017 Hydrocortisone Cream HYDROCORTISONE Trifecta Pharmaceuticals USA 4c96ec41-841c-322b-e054-00144ff8d46c 2025-05-08 Warnings Exact identifier application number: M017 GNP Extra Strength Anti-Itch Cream DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE Amerisource Bergen 34a66224-ef3c-e36e-e063-6394a90ac99d 2025-05-08 Warnings Exact identifier application number: M017 Good Neighbor Muscle Rub Cream CAMPHOR 4.0%, MENTHOL 10.0%, METHYL SALICYLATE 30.0%, Amerisource Bergen 34924bb9-e3e8-70e6-e063-6294a90aaa8c 2025-05-07 Warnings Exact identifier application number: M017 DermaRad Relief Post Radiation Calming LIDOCAINE 3 PERCENT Renu Laboratories, LLC e5d64929-fb9c-7ebc-e053-2995a90a9318 2025-05-07 Warnings Exact identifier application number: M017 Cold Hot Medicated Patch 5% Menthol MENTHOL InterMed Laboratories Private Limited 33ee0235-5a6e-0ea1-e063-6394a90a89a5 2025-05-06 Warnings Exact identifier application number: M017 DermaRad Relief LIDOCAINE EMULSION RENU LABORATORIES, LLC d5e11f73-918b-eeac-e053-2995a90a4a83 2025-05-06 Warnings Exact identifier application number: M017 Plantar Fasciitis Pain Relief Gel-Patch LIDOCAINE, MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 34838622-b092-afeb-e063-6294a90ae7db 2025-05-06 Warnings Exact identifier application number: M017 Climax Shield Delay BENZOCAINE PRODUCT MAX GROUP INC 9c720cdc-f753-47ce-95ff-3b26e461a0ab 2025-05-05 Warnings Exact identifier application number: M017 PediFix Lidocaine Pain-Relief Patches LIDOCAINE PAIN-RELIEF PATCHES PediFix, Inc 346550b9-d2ba-184e-e063-6394a90a591a 2025-05-05 Warnings Exact identifier application number: M017 Walgreens Stop Itch Gel DIPHENHYDRAMINE HCL Walgreens Co 23586336-8f46-3dcd-e063-6394a90accc9 2025-05-04 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