Home NDC 11822-6300 Nighttime 4X Medicated Cream
Product NDC 11822-6300
11-digit product format 118226300
Labeler code 11822
Product ID 11822-6300_441ef5c1-674c-f57e-e063-6394a90ab336
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form PASTE
Route ORAL
Labeler Rite Aid
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-12-01
Substance BENZALKONIUM CHLORIDE; BENZOCAINE; ZINC CHLORIDE; MENTHOL
Active strength .13; 20; .15; .26 g/100g; g/100g; g/100g; g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [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 Nighttime 4X Medicated Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 g/100g BENZOCAINE 20 g/100g ZINC CHLORIDE .15 g/100g MENTHOL .26 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2370903 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 11822-6300-1 Nighttime 4X Medicated Cream 7 g in 1 TUBE PASTE 7 3 11822-6300-1 Nighttime 4X Medicated Cream 1 in 1 CARTON PASTE 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-6300 NIGHTTIME 4X MEDICATED CREAM (BENZOCAINE) PASTE [RITE AID] 2 Current NDC, 2 package rows 20250124_21645ed1-2dc0-223a-e063-6394a90ab021.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 76 of 151 · 3,020 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 11822-6300-1 11822630001 1 TUBE in 1 CARTON (11822-6300-1) / 7 g in 1 TUBE 1 tube 2024-12-01 No No Current