Home NDC 55910-295 Itch Relief
Product NDC 55910-295
11-digit product format 559100295
Labeler code 55910
Product ID 55910-295_4c0f56dd-647f-bdfa-e063-6394a90aebb8
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl, Zinc Acetate
Dosage form SPRAY
Route TOPICAL
Labeler Old East Main Co.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-07-14
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength 20; 1 mg/mL; mg/mL
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 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 20 mg/mL ZINC ACETATE 1 mg/mL
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 1053138 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 55910-295-20 Itch Relief 59 mL in 1 BOTTLE, SPRAY SPRAY 59 17
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DIPHENHYDRAMINE HYDROCHLORIDE ACTIVE INGREDIENT TC2D6JAD40 ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3 ZINC ACETATE ACTIVE INGREDIENT FM5526K07A ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3 DIPHENHYDRAMINE ACTIVE MOIETY 8GTS82S83M ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3 ZINC CATION ACTIVE MOIETY 13S1S8SF37 ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3 POVIDONE INACTIVE INGREDIENT FZ989GH94E ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3 TROMETHAMINE INACTIVE INGREDIENT 023C2WHX2V ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3 WATER INACTIVE INGREDIENT 059QF0KO0R ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [DOLGENCORP, LLC] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-295 ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [OLD EAST MAIN CO] 15 Current NDC, Legacy NDC, 1 package rows 20240915_6d87547f-bf4c-4dda-bd9d-32b576afd805.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 113 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join HealthWise Medicated Foot Powder MENTHOL Veridian Healthcare 2916a0c3-2d66-d079-e063-6394a90acd6b 2024-12-12 Warnings Exact identifier application number: M017 Ease Your Pain MENTHOL Proximity Capital Partners LLC dba Asutra 83366ae1-e1d9-2a30-e053-2a91aa0a1cc4 2024-12-12 Warnings Exact identifier application number: M017 Natural Seal Itch Relief for Kids LIDOCAINE Kericure Inc. 31cc0c95-5864-4737-b085-8f58e00f4f05 2024-12-12 Warnings Exact identifier application number: M017 Vagisil Anti-Itch Creme Maximum Strength Sensitive Skin Formula HYDROCORTISONE ACETATE Combe Incorporated 9b69fa24-02dd-43e4-a81f-9a37968d7099 2024-12-12 Warnings Exact identifier application number: M017 VAGISIL Anti-Itch Medicated Creme Maximum Strength BENZOCAINE AND RESORCINOL Combe Incorporated bb73ebd7-ceb0-4b54-9e8f-77486d9037fb 2024-12-12 Warnings Exact identifier application number: M017 VAGISIL Anti-Itch Creme Regular Strength BENZOCAINE AND RESORCINOL Combe Incorporated dd303ff8-0deb-4292-bfd8-5bda91f86d51 2024-12-12 Warnings Exact identifier application number: M017 VAGISIL Anti-Itch Medicated Wipes Maximum Strength PRAMOXINE HYDROCHLORIDE Combe Incorporated b848f53d-8aea-4efe-aa2c-009d5121fc33 2024-12-12 Warnings Exact identifier application number: M017 Walgreens Cool and Heat MENTHOL 16% Walgreens ce1585f4-ca65-8d0c-e053-2995a90a8e89 2024-12-11 Warnings Exact identifier application number: M017 Walgreens Cool n Heat LIDOCAINE 4% Walgreens ce1b21d6-7aa6-2b18-e053-2995a90a4c91 2024-12-11 Warnings Exact identifier application number: M017 Walgreens Pain Burn Itch Relief BENZOCAINE 20%, MENTHOL 0.5% Walgreens cc6e4b42-fdd8-6ff7-e053-2995a90a3d1d 2024-12-11 Warnings Exact identifier application number: M017 Pramoxine Itch relief PRAMOXINE HCL 1% CVS e947694c-c122-0291-e053-2995a90ac39a 2024-12-11 Warnings Exact identifier application number: M017 Arthritis Cream TROLAMINE SALICYLATE 10% CVS d1663f50-479b-4d55-e053-2995a90a223f 2024-12-11 Warnings Exact identifier application number: M017 CVS Pain Relief MENTHOL 4% CVS d1660d55-1ee0-7aa2-e053-2995a90a6579 2024-12-11 Warnings Exact identifier application number: M017 CVS Muscle Rub MENTHOL 10%, METHYL SALICYLATE 15% CVS Health c72c9a95-4226-6d69-e053-2a95a90a8e1c 2024-12-11 Warnings Exact identifier application number: M017 BENGAY ULTRA STRENGTH NON-GREASY CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE Kenvue Brands LLC 0a41ec65-bd0b-4fc6-807d-74f353341cc7 2024-12-11 Warnings Exact identifier application number: M017 Serum X LIDOCAINE HYDROCHLORIDE AO Biologix, LLC e07b6268-6400-6849-e053-2a95a90a8b3e 2024-12-11 Warnings Exact identifier application number: M017 PlusCBD Pain Cream (Penetrating) 2oz CAMPHOR, MENTHOL CV Sciences, Inc. ca39d327-6bf3-3408-e053-2a95a90af2d5 2024-12-11 Warnings Exact identifier application number: M017 Blistex Medicated DIMETHICONE, CAMPHOR (SYNTHETIC), MENTHOL, AND PHENOL Blistex Inc. e95439d3-f12b-4c1c-999a-79f2ddba4cfb 2024-12-11 Warnings Exact identifier application number: M017 Blistex Foille Medicated First Aid BENZOCAINE AND CHLOROXYLENOL Blistex Inc. e2eca808-e97b-43e0-aa51-7025cc61c7a8 2024-12-11 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE J&A Digital Inc. ff95a536-35b3-4006-b43c-cce359e86aa9 2024-12-10 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 55910-295-20 55910029520 59 mL in 1 BOTTLE, SPRAY (55910-295-20) 59 ml 2010-07-14 0000-00-00 No No Current