Home NDC 11822-2215 Maximum Strength Scalp Itch Relief
Product NDC 11822-2215
11-digit product format 118222215
Labeler code 11822
Product ID 11822-2215_bf331cf8-b6ca-41ce-b7ca-2dde91c917d6
Type HUMAN OTC DRUG
Nonproprietary name HYDROCORTISONE
Dosage form LIQUID
Route TOPICAL
Labeler Rite Aid
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-09
Substance HYDROCORTISONE
Active strength 10 mg/mL
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 Maximum Strength Scalp Itch Relief
Brand name suffix Anti-itch
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE 10 mg/mL
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 310869 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 11822-2215-1 Maximum Strength Scalp Itch ReliefAnti-itch 1 in 1 CARTON LIQUID 1 2 11822-2215-1 Maximum Strength Scalp Itch ReliefAnti-itch 74 mL in 1 BOTTLE, DISPENSING LIQUID 74 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-2215 MAXIMUM STRENGTH SCALP ITCH RELIEF ANTI-ITCH (HYDROCORTISONE) LIQUID [RITE AID] 1 Current NDC, 2 package rows 20240302_55569563-fc38-4f97-8e74-9f96e3173384.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 18 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 11822-2215-1 11822221501 1 BOTTLE, DISPENSING in 1 CARTON (11822-2215-1) / 74 mL in 1 BOTTLE, DISPENSING 2024-02-09 No No Current