Home NDC 84573-547 Real Time Pain Relief Maxx Plus Topical Analgesic
Product NDC 84573-547
11-digit product format 845730547
Labeler code 84573
Product ID 84573-547_26b61417-67ca-df12-e063-6394a90a79ef
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form LOTION
Route TOPICAL
Labeler Real Time Products Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-10-23
Substance MENTHOL
Active strength 19 mg/mL
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 Real Time Pain Relief Maxx Plus Topical Analgesic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 19 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII 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 84573-547-03 Real Time Pain Relief Maxx Plus Topical Analgesic 88 mL in 1 TUBE LOTION 88 1 84573-547-04 Real Time Pain Relief Maxx Plus Topical Analgesic 120 mL in 1 TUBE LOTION 120 1 84573-547-05 Real Time Pain Relief Maxx Plus Topical Analgesic 147.8 mL in 1 TUBE LOTION 147.8 1 84573-547-07 Real Time Pain Relief Maxx Plus Topical Analgesic 210 mL in 1 TUBE LOTION 210 1 84573-547-12 Real Time Pain Relief Maxx Plus Topical Analgesic 354 mL in 1 BOTTLE LOTION 354 1 84573-547-16 Real Time Pain Relief Maxx Plus Topical Analgesic 473 mL in 1 BOTTLE LOTION 473 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84573-547 REAL TIME PAIN RELIEF MAXX PLUS TOPICAL ANALGESIC (MENTHOL) LOTION [REAL TIME PRODUCTS INC.] 1 Current NDC, 6 package rows 20241114_fc509a55-594d-4d44-87db-33286e937581.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 108 of 151 · 3,020 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84573-547-03 84573054703 88 mL in 1 TUBE (84573-547-03) 88 ml 2024-10-23 No No Current 84573-547-04 84573054704 120 mL in 1 TUBE (84573-547-04) 120 ml 2024-10-23 No No Current 84573-547-05 84573054705 147.8 mL in 1 TUBE (84573-547-05) 147.8 ml 2024-10-23 No No Current 84573-547-07 84573054707 210 mL in 1 TUBE (84573-547-07) 210 ml 2024-10-23 No No Current 84573-547-12 84573054712 354 mL in 1 BOTTLE (84573-547-12) 354 ml 2024-10-23 No No Current 84573-547-16 84573054716 473 mL in 1 BOTTLE (84573-547-16) 473 ml 2024-10-23 No No Current