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 27 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SPARTAN LIDOCAINE TIV PRIME SRL 4e04146a-ed19-2271-e063-6394a90a50f0 2026-03-27 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Lidocaine LIDOCAINE Walgreen Co. 41d5bdc4-66c8-31ab-e063-6394a90a1195 2026-03-27 Warnings Exact identifier application number: M017 Walgreens Cool N Heat Patch LIDOCAINE, MENTHOL Walgreen Co. 41d64a88-90fc-27ca-e063-6294a90a602b 2026-03-27 Warnings Exact identifier application number: M017 Softlips Naturals Medicated CAMPHOR, MENTHOL The Mentholatum Company 4e05d134-6c7f-1501-e063-6294a90ad27d 2026-03-27 Warnings Exact identifier application number: M017 Walgreens Cool N Heat Patch XL MENTHOL Walgreen Co. 41e92435-7f77-a593-e063-6394a90a4b38 2026-03-27 Warnings Exact identifier application number: M017 Walgreens Cool N Heat Back Patch MENTHOL Walgreen Co. 41e81110-4b79-1fa6-e063-6394a90ae90c 2026-03-27 Warnings Exact identifier application number: M017 Softlips Naturals Medicated Elderberry Acai CAMPHOR, MENTHOL The Mentholatum Company 4e0743a6-d450-043b-e063-6394a90ad1c2 2026-03-27 Warnings Exact identifier application number: M017 QFSN Pain Relief Cream PAIN RELIEF CREAM Qiaofusheng Pharmaceuticals Co., Ltd. 4d215da1-87f5-d35d-e063-6394a90ac348 2026-03-27 Warnings Exact identifier application number: M017 FlexSport Roll On METHYL SALICYLATE Pharmadel LLC bf8de3da-7628-6112-e053-2995a90a8e16 2026-03-26 Warnings Exact identifier application number: M017 Kofal Original METHYL SALICYLATE Pharmadel LLC 984780fd-496b-150b-e053-2995a90aed77 2026-03-26 Warnings Exact identifier application number: M017 Kofal Fuerte METHYL SALICYLATE Pharmadel LLC 98488a07-eba0-2b4e-e053-2995a90ad6ab 2026-03-26 Warnings Exact identifier application number: M017 Kofal Max Power MENTHOL Pharmadel LLC fe1f1408-b0cb-67a4-e053-6394a90ad609 2026-03-26 Warnings Exact identifier application number: M017 Kofal METHYL SALICYLATE Pharmadel LLC 9cac377d-97bc-f0b7-e053-2a95a90a2e12 2026-03-26 Warnings Exact identifier application number: M017 Milagroso CAMPHOR Pharmadel LLC 12b0401c-84d5-07cd-e063-6394a90a052c 2026-03-26 Warnings Exact identifier application number: M017 Ubredol METHYL SALICYLATE Pharmadel LLC fe96eead-1722-c05d-e053-6394a90a850f 2026-03-26 Warnings Exact identifier application number: M017 DZUL PAIN FREEZE INSTANT PAIN RELIEF MENTHOL Caball Sales, Inc. 4df3abcc-17f3-17f2-e063-6294a90afcca 2026-03-26 Warnings Exact identifier application number: M017 Equate Cool and Heat Extra Strength MENTHOL Wal-Mart Stores Inc ca3088a7-e1ec-4e69-80d9-fd0051bde938 2026-03-25 Warnings Exact identifier application number: M017 Ultra Strength Muscle Rub - CVS Health Ultra Strength Muscle Rub CAMPHOR, MENTHOL, METHYL SALICYLATE CVS Pharmacy 2ea95529-ec4b-c2ce-e063-6394a90a0739 2026-03-25 Warnings Exact identifier application number: M017 NUMBING CREAMS MENTHOL LIDOCAINE Yongchun Lihui Trading Co., Ltd. 4dd38cdf-d644-6da0-e063-6294a90afb3d 2026-03-25 Warnings Exact identifier application number: M017 ANTIPHLAMINE L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE Masaem Company 4dd3ab12-6cd3-1060-e063-6394a90a2dec 2026-03-25 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