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 146 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Alo Therapeutic Massage MENTHOL, HISTAMINE DIHYDROCHLORIDE CMI Therapy Solutions 40f92e71-fe2e-16f4-e054-00144ff8d46c 2023-11-10 Warnings Exact identifier application number: M017 Teeter Renew Muscles Pain Relieving METHYL SALICYLATE, MENTHOL STL International INC b90dc5b9-c31d-4770-a291-98d036ae8723 2023-11-10 Warnings Exact identifier application number: M017 SMOOTH GATOR Foot and Leg Rub CAMPHOR (SYNTHETIC), MENTHOL Smooth Gator LLC 57094238-506b-48c1-8eb9-fe904be80df0 2023-11-10 Warnings Exact identifier application number: M017 SKIN A COOL Hydrocortisone Anti-Itch HYDROCORTISONE Ana-Cool, LLC e3ea7406-e494-4038-9b28-8d0a28b4b834 2023-11-10 Warnings Exact identifier application number: M017 Teeter reNEW MUSCLES Pain Relieving METHYL SALICYLATE, MENTHOL STL International INC ebc777b0-d141-4a62-9366-d14787eaefe0 2023-11-10 Warnings Exact identifier application number: M017 FEELGOOD LAB Natural Pain Cream MENTHOL The Feel Good Lab, LLC 799d464c-aaf1-429a-877b-2a692397bb49 2023-11-10 Warnings Exact identifier application number: M017 HIGHER CONTROL Male Climax Control Lubricating BENZOCAINE Product Max Group Inc 5f5fd127-34c5-403a-aa95-c9874ae79492 2023-11-10 Warnings Exact identifier application number: M017 Alo Therapeutic Massage MENTHOL, HISTAMINE DIHYDROCHLORIDE CMI Therapy Solutions 40f93076-1f68-58e6-e054-00144ff88e88 2023-11-10 Warnings Exact identifier application number: M017 Alo Therapeutic Massage MENTHOL, HISTAMINE DIHYDROCHLORIDE CMI Therapy Solutions 40f9622e-27c7-6a5d-e054-00144ff88e88 2023-11-10 Warnings Exact identifier application number: M017 FEEL GOOD LAB Natural Pain Cream MENTHOL THE FEEL GOOD LAB, LLC 774a72b1-b719-4217-846e-7f9921fd1b16 2023-11-10 Warnings Exact identifier application number: M017 BODY ACTION PRODUCTS Climax Control Gel BENZOCAINE PRODUCT MAX GROUP INC 53e746cc-0078-4381-bf0b-9c8f98d66904 2023-11-10 Warnings Exact identifier application number: M017 BODY ACTION PRODUCTS Endless Love for Men BENZOCAINE PRODUCT MAX GROUP INC d0fa792d-dc04-4bdf-a22d-dea896beae5b 2023-11-10 Warnings Exact identifier application number: M017 Endless Love For Men BENZOCAINE Body Action Products, Inc 4e89cd3a-ecad-44c3-acb3-6d0810add8c0 2023-11-10 Warnings Exact identifier application number: M017 BODY ACTION PRODUCTS Higher Control Male Climax BENZOCAINE PRODUCT MAX GROUP INC 3c7fa73b-abe8-4a8d-951c-4e785d6e812c 2023-11-10 Warnings Exact identifier application number: M017 Uber Numb LIDOCAINE HYDROCHLORIDE UBERScientific, LLC 65a319a6-89d2-44c9-81d5-30327f9948cb 2023-11-10 Warnings Exact identifier application number: M017 Uber Numb LIDOCAINE HYDROCHLORIDE UBERScientific, LLC 768f3f0e-1add-404f-b869-00a9f35ad34a 2023-11-10 Warnings Exact identifier application number: M017 Zcaine Fast Acting Anesthetic LIDOCAINE PHI, Inc d072243f-6ba6-4ab6-8ebf-a2381fa9c2df 2023-11-09 Warnings Exact identifier application number: M017 Plum Smooth Plumb Numb Gelee LIDOCAINE Universal Companies, Inc. 6be7d8e0-6cd0-4da2-926f-3dbb3db3bd8e 2023-11-09 Warnings Exact identifier application number: M017 Sonacaine Topical Anesthetic With Menthol LIDOCAINE Filltech USA, LLC ca54c6da-4bf2-4e63-ba7f-a69c4f9c431a 2023-11-09 Warnings Exact identifier application number: M017 Bed Bug Instant Bite Relief LIDOCAINE P.F. Harris Mfg. Co. LLC 7f472fd0-5605-4cc6-b4b2-1267e815255c 2023-11-09 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