Home NDC 55910-225 rexall anti itch
Product NDC 55910-225
11-digit product format 559100225
Labeler code 55910
Product ID 55910-225_81484ab5-e657-4297-ad8d-00f24c3ec0e8
Type HUMAN OTC DRUG
Nonproprietary name Hydrocortisone
Dosage form CREAM
Route TOPICAL
Labeler Dolgencorp, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-08-31
Substance HYDROCORTISONE
Active strength 1 g/100g
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 rexall anti itch
Brand name suffix maximum strength relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WI4X0X7BPJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 106258 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 55910-225-64 rexall anti itchmaximum strength relief 28 g in 1 TUBE CREAM 28 7 55910-225-64 rexall anti itchmaximum strength relief 1 in 1 CARTON CREAM 1 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded HYDROCORTISONE ACTIVE INGREDIENT WI4X0X7BPJ REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 HYDROCORTISONE ACTIVE MOIETY WI4X0X7BPJ REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 BUTYLATED HYDROXYTOLUENE INACTIVE INGREDIENT 1P9D0Z171K REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 CETOSTEARYL ALCOHOL INACTIVE INGREDIENT 2DMT128M1S REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 CETYL ALCOHOL INACTIVE INGREDIENT 936JST6JCN REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 CHAMOMILE INACTIVE INGREDIENT FGL3685T2X REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 DIAZOLIDINYL UREA INACTIVE INGREDIENT H5RIZ3MPW4 REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 DIMETHICONE INACTIVE INGREDIENT 92RU3N3Y1O REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 DISTEARYLDIMONIUM CHLORIDE INACTIVE INGREDIENT OM9573ZX3X REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 GLYCERYL MONOSTEARATE INACTIVE INGREDIENT 230OU9XXE4 REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 HYDROLYZED JOJOBA ESTERS (ACID FORM) INACTIVE INGREDIENT UDR641JW8W REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 MAGNESIUM ASCORBYL PHOSPHATE INACTIVE INGREDIENT 0R822556M5 REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 MENTHYL LACTATE, (-)- INACTIVE INGREDIENT 2BF9E65L7I REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 METHYL GLUCETH-20 INACTIVE INGREDIENT J3QD0LD11P REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 OAT INACTIVE INGREDIENT Z6J799EAJK REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 POLYSORBATE 60 INACTIVE INGREDIENT CAL22UVI4M REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 POTASSIUM HYDROXIDE INACTIVE INGREDIENT WZH3C48M4T REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 STEARETH-2 INACTIVE INGREDIENT V56DFE46J5 REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 STEARETH-21 INACTIVE INGREDIENT 53J3F32P58 REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 STEARYL ALCOHOL INACTIVE INGREDIENT 2KR89I4H1Y REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 VITAMIN A PALMITATE INACTIVE INGREDIENT 1D1K0N0VVC REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2 WATER INACTIVE INGREDIENT 059QF0KO0R REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-225 REXALL ANTI ITCH MAXIMUM STRENGTH RELIEF (HYDROCORTISONE) CREAM [DOLGENCORP, LLC] 7 Current NDC, Legacy NDC, 2 package rows 20241004_894cf9ab-693a-4210-96df-605947f51b63.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 51 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join PREMIERES PAIN MENTHOL Premiere Enterprises 35ff19df-4cc4-4fce-bd30-d87d835e0e26 2025-12-23 Warnings Exact identifier application number: M017 Premieres Pain MENTHOL Premiere Enterprises 1f081913-6106-4d06-a37a-631f710dbacb 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE jr. LIDOCAINE HCL, PHENOL Clarion Brands, LLC e1de73bb-917c-48d1-9a78-00c76edddb98 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE jr. PLUS Knee CAMPHOR, MENTHOL Clarion Brands, LLC 3ad8718d-ebf1-474f-8a91-48c78ab3b5c1 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr. Plus MENTHOL Clarion Brands, LLC fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE JR PLUS ULTRA STRENGTH PAIN MENTHOL Clarion Brands, LLC cf329707-d90a-29dd-f2c2-acfd5af614f3 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr Pro Cream LIDOCAINE HCL, PHENOL Clarion Brands, LLC 17b3f1e6-5554-4f3e-b133-76ae8ffea919 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr Pro No Mess Roll-on Plus LIDOCAINE HCL, PHENOL Clarion Brands, LLC a7172f17-1525-4738-b72c-92479c730af2 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE JR MENTHOL Clarion Brands, LLC d656e7f6-ca26-1873-6c11-08aa82091bb0 2025-12-23 Warnings Exact identifier application number: M017 Relief Recovery METHYL SALICYLATE Mayway Corporation 27afd45e-2dc5-d099-e063-6394a90ad2b7 2025-12-23 Warnings Exact identifier application number: M017 Mobility METHYL SALICYLATE Mayway Corporation 27af9d17-9c15-5e2a-e063-6394a90aeda5 2025-12-23 Warnings Exact identifier application number: M017 medlot pain relief gel patch LIDOCAINE Lotfancy, Inc. 3ce4af20-b227-5b98-e063-6394a90ab992 2025-12-23 Warnings Exact identifier application number: M017 Nizoral Scalp Itch Relief HYDROCORTISONE Kramer Laboratories dba59238-6beb-447e-8c4c-e4bc00fd2c20 2025-12-23 Warnings Exact identifier application number: M017 Salonpas LIDOCAINE Pain Relieving LIDOCAINE Hisamitsu America, Inc. 63911880-8194-4c7d-a72f-cab94761b2d7 2025-12-23 Warnings Exact identifier application number: M017 The Body Builders Cream MENTHOL Smart Cookie Solutions f803325e-eb86-4b9e-a401-0a91bdcd6389 2025-12-22 Warnings Exact identifier application number: M017 PROINNATE Numbing Cream LIDOCAINE,MENTHOL Guangdong Aimu Biological Technology Co., Ltd 46895ddb-0b9f-675e-e063-6394a90adf23 2025-12-22 Warnings Exact identifier application number: M017 Caring Mills Vaginal Anti-Itch Cream BENZOCAINE, RESORCINOL Veridian Healthcare f2362658-aea2-438e-a66c-738022e6e047 2025-12-22 Warnings Exact identifier application number: M017 HealthWise Pain Relieving Menthol Gel MENTHOL 2% Veridian Healthcare 396d0fd4-67be-4de1-8f0c-42c83dfe9120 2025-12-22 Warnings Exact identifier application number: M017 Large Medicate Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Amerisource Bergen a7d5f89b-59b9-4603-99aa-273b85be813e 2025-12-22 Warnings Exact identifier application number: M017 Good Neighbor Capsaicin Heat Patch for Back CAPSAICIN Amerisource Bergen f873a0b8-8123-1600-e053-6394a90a043e 2025-12-22 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 55910-225-64 55910022564 1 TUBE in 1 CARTON (55910-225-64) / 28 g in 1 TUBE 1 tube 2010-08-31 0000-00-00 No No Current