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 99 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tylenol Precise Nighttime Pain Relieving CAMPHOR, MENTHOL Kenvue Brands LLC 2ef4fe16-0820-6aad-e063-6294a90a8449 2025-02-25 Warnings Exact identifier application number: M017 LidoPro Pain Relief CAPSAICIN AND LIDOCAINE Preferred Pharmaceuticals Inc. c259ef92-5d07-4590-adf1-3a106333eee0 2025-02-21 Warnings Exact identifier application number: M017 Cortizone 10 Ultra Soothing Itch Relief HYDROCORTISONE Chattem, Inc. 8a9e2d32-a65f-4253-8041-4146f4e3b738 2025-02-21 Warnings Exact identifier application number: M017 AVCOO Pain Relief Roll On MENTHOL ADP Health Limited 420d8cdc-f47f-4d33-bf25-9033ff266c49 2025-02-19 Warnings Exact identifier application number: M017 AVCOO Pain Relief MENTHOL ADP Health Limited 700ce2cf-749e-40be-91c3-850d9b2168ca 2025-02-19 Warnings Exact identifier application number: M017 Sunburn Relief Gel LIDOCAINE HCL Jell Pharmaceuticals Pvt. Ltd 2e7c49de-5438-4858-e063-6294a90ad98c 2025-02-19 Warnings Exact identifier application number: M017 VTROUY Tattoo Numbing Cream TATTOO NUMBING CREAM Guangzhou Zanming Trading Co., Ltd. 2e899851-b3cd-0758-e063-6294a90afea8 2025-02-19 Warnings Exact identifier application number: M017 Pomada Dragon Pain Relief MENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC), AND METHYL SALICYLATE Genomma Lab USA 9d98f48b-6d88-4df9-9459-7cf7ba5de044 2025-02-19 Warnings Exact identifier application number: M017 Pain Relieving Cream HISTAMINE DIHYDROCHLORIDE Mediapower, Inc. DBA Dr Newton's And Naturals 9eeea033-ae87-4d83-85d0-b8fa653a0806 2025-02-19 Warnings Exact identifier application number: M017 Sure Complete Confidence Antiperspirant Deodorant Aerosol, Regular ALUMINUM CHLOROHYDRATE Sodalis USA, LLC 7839cf53-dbd2-4dbb-a309-1581d51f8adc 2025-02-18 Warnings Exact identifier application number: M017 CANNA NUMB Roll On LIDOCAINE HYDROCHLORIDE, MENTHOL Cannanumb LLC c1eb0348-3b0e-4f1c-a46b-1ff4aa165fb4 2025-02-17 Warnings Exact identifier application number: M017 Vaporizing Chest Rub 4 oz. CAMPHOR, EUCALYPTUS OIL, MENTHOL Rejoice International Inc. 7173b141-123e-6cd4-e053-2a95a90a8600 2025-02-12 Warnings Exact identifier application number: M017 Vaporizing Chest Rub 4 oz. 3 pk CAMPHOR, EUCALYPTUS OIL, MENTHOL Rejoice International Inc. 71c186a1-8283-2482-e053-2995a90acc1f 2025-02-12 Warnings Exact identifier application number: M017 Roman Swipes BENZOCAINE Roman Health Ventures Inc. 7f0eac8c-7235-99d8-e053-2a91aa0a634e 2025-02-12 Warnings Exact identifier application number: M017 SANAR NATURAL-ARNICA ROLL ON ARNICA PAIN RELIEVING WITH CAMPHOR EVI LABS EVI LABS 2df7658d-83d3-41ac-e063-6294a90ab1dd 2025-02-12 Warnings Exact identifier application number: M017 Signature Care Medicated Pain Relief Patch LIDOCAINE Safeway, Inc. 2165a342-5f8b-78e0-e063-6394a90a06c4 2025-02-12 Warnings Exact identifier application number: M017 CheeZheng Pain Relieveing Plaster CAMPHOR Tibet Cheezheng Tibetan Medicine Co. Ltd. abcebdf1-9037-4094-93e1-ce8f20b18ea7 2025-02-11 Warnings Exact identifier application number: M017 Tibetree Pain Relieveing Medicated Plaster CAMPHOR Tibet Cheezheng Tibetan Medicine Co. Ltd 4216bd48-5c62-4e87-adcc-67bf7152d64d 2025-02-11 Warnings Exact identifier application number: M017 AsperFlex LIDOCAINE Akron Pharma Inc. ab50525e-b534-452b-8c25-2992c0cbf862 2025-02-10 Warnings Exact identifier application number: M017 Olu Pain Management LIDOCAINE AND CAMPHOR Olakino Therapeutics LLC 2a41a621-c6f7-5819-e063-6394a90ae67d 2025-02-07 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