Home NDC 84804-321 NanoXtreme Pain Relieving
Product NDC 84804-321
11-digit product format 848040321
Labeler code 84804
Product ID 84804-321_23e5ef27-3808-fc0c-e063-6394a90acbe4
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, METHYL SALICYLATE
Dosage form CREAM
Route TOPICAL
Labeler MG Science Technologies LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-11-23
Substance MENTHOL; METHYL SALICYLATE
Active strength 40; 100 mg/mL; 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 NanoXtreme Pain Relieving
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 40 mg/mL METHYL SALICYLATE 100 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup LAV5U5022Y Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2698214 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84804-321-01 NanoXtreme Pain Relieving 100 mL in 1 TUBE CREAM 100 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84804-321 NANOXTREME PAIN RELIEVING (MENTHOL, METHYL SALICYLATE) CREAM [MG SCIENCE TECHNOLOGIES LLC] 2 Current NDC, 1 package rows 20241123_c1490c30-a9db-4120-adaf-9e8000169e46.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 8 of 156 · 3,115 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 84804-321-01 84804032101 100 mL in 1 TUBE (84804-321-01) 100 ml 2024-11-23 No No Current