Home NDC 72037-136 AcuPlus Advanced Therapy for Pain and Recovery
Product NDC 72037-136
11-digit product format 720370136
Labeler code 72037
Product ID 72037-136_0974c990-eb0f-73ff-e063-6294a90af414
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form SOLUTION
Route TOPICAL
Labeler INNOVATIONS FOR WELLNESS, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-05-01
Substance MENTHOL
Active strength 35 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 AcuPlus Advanced Therapy for Pain and Recovery
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 35 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1089766 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 72037-136-03 AcuPlus Advanced Therapy for Pain and Recovery 89 mL in 1 TUBE SOLUTION 89 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72037-136 ACUPLUS ADVANCED THERAPY FOR PAIN AND RECOVERY (MENTHOL) SOLUTION [INNOVATIONS FOR WELLNESS, LLC] 2 Current NDC, Legacy NDC, 1 package rows 20231106_840cfd15-4ea1-49bf-8c4f-86c12461d860.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 · 3,010 matching rows.
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 72037-136-03 72037013603 89 mL in 1 TUBE (72037-136-03) 89 ml 2019-05-01 0000-00-00 No No Current