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 82 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Aruba Aloe Alcoholada LIDOCAINE HYDROCHLORIDE Aruba Aloe Balm NV f56c62b0-75db-4499-858e-54e10b0e140a 2025-08-07 Warnings Exact identifier application number: M017 SurviveX Hydrocortisone Cream HYDROCORTISONE Nantong Health & Beyond Hygienic Products Inc. 3bd1da8d-5142-798c-e063-6294a90a7be6 2025-08-07 Warnings Exact identifier application number: M017 Arthcal SOOTHING PAIN RELIEF MASSAGE SOOTHING PAIN RELIEF MASSAGE Beijing JUNGE Technology Co., Ltd. 3524ad62-0ed6-f2e5-e063-6394a90a3283 2025-08-06 Warnings Exact identifier application number: M017 Alumier MD Intensive Recovery HYDROCORTISONE Alumier Labs d9b79ea1-6558-543c-e053-2995a90ae53e 2025-08-06 Warnings Exact identifier application number: M017 Good Neighbor Roll-on Pain Relief LIDOCAINE HCL Amerisource Bergen a0c3adbf-fa35-47c0-9db3-459ce9a106ac 2025-08-06 Warnings Exact identifier application number: M017 Good Neighbor Roll-on Menthol Pain Relief Gel MENTHOL Amerisource Bergen bd557323-0003-4ee6-b22d-a72d621c7de4 2025-08-05 Warnings Exact identifier application number: M017 Earthmed FS Pain relieving balm MENTHOL Earthmed LLC 3ba4e769-fec6-52d9-e063-6394a90a65d4 2025-08-05 Warnings Exact identifier application number: M017 HYDROCORTISONE HYDROCORTISONE HF Acquisition Co LLC, DBA HealthFirst 3ba6a5ec-fda2-b2a6-e063-6294a90ac9b6 2025-08-05 Warnings Exact identifier application number: M017 Kocowo Lidocaine Pain Relief Gel-Patch LIDOCAINE PAIN RELIEF GEL-PATCH Henan Enokon Medical Instrument Co., Ltd. 3b82989d-7cc3-23d3-e063-6294a90ae2a3 2025-08-03 Warnings Exact identifier application number: M017 Menthol pain relief patches MENTHOL Menthol pain relief patch 3b5fd718-3f86-f7a7-e063-6294a90a8c52 2025-08-02 Warnings Exact identifier application number: M017 Graphene Far Infrared Herbal Pain Relief Patches CORYDALIS RHIZOME Changsha Maocheng Trading Co., Ltd 3b604a3c-fe91-7096-e063-6394a90afe04 2025-08-02 Warnings Exact identifier application number: M017 Active Recovery Pain Relief CAMPHOR, MENTHOL Charlotte's Web, Inc. 3a9f9ca0-3d8a-796a-e063-6394a90a790c 2025-08-01 Warnings Exact identifier application number: M017 Active Recovery Pain Relief Stick CAMPHOR, MENTHOL Charlottes Web, Inc. 3aa037c6-6109-b52e-e063-6394a90a215b 2025-08-01 Warnings Exact identifier application number: M017 PM Recovery Pain Relief CAMPHOR, MENTHOL Charlotte's Web, Inc. 3aa08859-809d-de8c-e063-6394a90a8e25 2025-08-01 Warnings Exact identifier application number: M017 Wish ultra winter ice MENTHOL LJ Pharma b4c5487c-1314-4d63-96df-077e72e7ee95 2025-08-01 Warnings Exact identifier application number: M017 Rugged Fit Pain Relief Roll On MENTHOL, METHYL SALICYLATE SYSTEM4BOOK LLC 39d68734-981c-14d7-e063-6294a90a4919 2025-08-01 Warnings Exact identifier application number: M017 ICY FREEZE MENTHOL, UNSPECIFIED FORM Natural Essentials, Inc. 28fdb049-b297-4358-9447-7d69ba879702 2025-08-01 Warnings Exact identifier application number: M017 Cortizone 10 Cooling HYDROCORTISONE Chattem, Inc. 14d9fce2-9f54-4204-83cb-161de8a303f0 2025-08-01 Warnings Exact identifier application number: M017 Bravado Labs Numbing LIDOCAINE HCL Prodigy Media Inc 8c43f5b5-b911-4a7a-b2d1-56a09c54b001 2025-07-30 Warnings Exact identifier application number: M017 Chimera GUARD LIDOCAINE PAIN RELIEFING PATCH Hangzhou Rongna Health Technology Co., Ltd. 3721c984-1993-6265-e063-6394a90af23f 2025-07-29 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