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 104 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Lidocare Arm, Neck, Leg 4% LIDOCAINE Kingsway Pharmaceuticals dba NFI, LLC 59a104ee-7034-99c3-e053-2991aa0a164c 2025-01-06 Warnings Exact identifier application number: M017 Salonpas LIDOCAINE Pain Relieving LIDOCAINE Hisamitsu Pharmaceutical Co., Inc. 4f3a438c-f378-4d2a-a95c-58e56cf1e797 2025-01-06 Warnings Exact identifier application number: M017 Lidocare 03 4% LIDOCAINE Kingsway Pharmaceuticals dba NFI, LLC 416ebf5a-2efb-6d0b-e054-00144ff88e88 2025-01-06 Warnings Exact identifier application number: M017 AVCOO Pain Relief Roll-on MENTHOL ADP Health Limited e0bb77b2-45ee-45fa-9659-9c7d99bb20dc 2025-01-05 Warnings Exact identifier application number: M017 health and beyond BURN LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE Nantong Health & Beyond Hygienic Products Inc. 0b6bb3ed-50fb-40c4-acb6-ae3f16031531 2025-01-05 Warnings Exact identifier application number: M017 glo SKIN BEAUTY Remedy Gel GLO SKIN BEAUTY REMEDY GEL Hayden Caleel LLC aa47ff08-07b3-4fd1-bae5-420e4b928f06 2025-01-05 Warnings Exact identifier application number: M017 Capsaicin 0.025% Cream CAPSAICIN 0.025% Puretek Corporation 28f00df0-c416-f17b-e063-6294a90a5570 2025-01-02 Warnings Exact identifier application number: M017 AVON HeXashield Pain Relief for Muscle, Back and Joint Cream CAMPHOR, MENTHOL, METHYL SALICYLATE Tai Guk Pharm. Co., Ltd. 8f29ffd7-48b9-109f-e053-2995a90ab215 2025-01-01 Warnings Exact identifier application number: M017 AVON HeXashield Arthritis Pain Relief Cream Capsaisin CAPSAISIN Tai Guk Pharm. Co., Ltd. 8f286a9d-8765-21b3-e053-2a95a90ae43a 2025-01-01 Warnings Exact identifier application number: M017 AVON HeXashield Anti Itch Cream with Healing Aloe HYDROCORTISONE Tai Guk Pharm. Co., Ltd. 8f2aa11d-d794-6f3e-e053-2995a90a1d9d 2025-01-01 Warnings Exact identifier application number: M017 HeXashield Anti Itch Cream with Healing Aloe HYDROCORTISONE Tai Guk Pharm. Co., Ltd. b9d033f3-4d12-a2c8-e053-2995a90ac7f1 2025-01-01 Warnings Exact identifier application number: M017 Green Compass Reduce Pain Relief with Menthol MENTHOL Green Compass, Inc. 0a0c212e-ae5d-8505-e063-6394a90af622 2025-01-01 Warnings Exact identifier application number: M017 Green Compass Reduce Pain Relief CAMPHOR, MENTHOL, METHYL SALICYLATE Green Compass, Inc. 0a0b688e-50f1-3eb1-e063-6394a90a7efa 2025-01-01 Warnings Exact identifier application number: M017 Green Compass Reduce Topical Pain CAMPHOR, MENTHOL, METHYL SALICYLATE Green Compass, Inc. 8cb80362-5d24-1ee3-e053-2a95a90afcdf 2025-01-01 Warnings Exact identifier application number: M017 OKeeffes Working Hands Pain Relief Skin Protectant ALLANTOIN, LIDOCAINE HYDROCHLORIDE The Gorilla Glue Company/O'Keeffe's Company 0685da25-c9fa-e1cd-e063-6394a90ae1b3 2025-01-01 Warnings Exact identifier application number: M017 Icy Hot with Lidocaine Pain Relieving LIDOCAINE HCL AND MENTHOL Chattem, Inc. 75b28b06-77ea-4fea-b516-2e8a0dac7037 2025-01-01 Warnings Exact identifier application number: M017 Advanced Seal Barrier plus Pain Relief LIDOCAINE Kericure Inc. 7ac95325-e6e9-4c56-9315-876c00af7c98 2025-01-01 Warnings Exact identifier application number: M017 FixMySkin Healing Balm Fragrance-Free HYDROCORTISONE Lovely Skin, Inc. c12af4c6-2f05-46ec-b901-1a4fcd750180 2024-12-31 Warnings Exact identifier application number: M017 Pain Relieving Cream Lidocaine BENZYL ALCOHOL, LIDOCAINE HCI Trifecta Pharmaceuticals USA LLC 039a2036-54b2-cf28-e063-6294a90a8ce6 2024-12-31 Warnings Exact identifier application number: M017 Cold Therapy Pain Relief Walgreens MENTHOL 10.5% WALGREEN COMPANY f1daa68d-1b12-c28a-e053-2995a90a0949 2024-12-31 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