Home NDC 76348-971 MG PLUS ROLL ON
Product NDC 76348-971
11-digit product format 763480971
Labeler code 76348
Product ID 76348-971_535dc42f-38c8-2afc-e063-6294a90ae23d
Type HUMAN OTC DRUG
Nonproprietary name Menthol Roll On
Dosage form LIQUID
Route TOPICAL
Labeler RENU LABORATORIES, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-08
Substance MENTHOL
Active strength 4.2 g/84g
NDC exclude flag No
Listing certified through 2027-12-31
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 MG PLUS ROLL ON
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 4.2 g/84g
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.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 76348-971-03 76348097103 84 g in 1 BOTTLE, WITH APPLICATOR (76348-971-03) 84 g 2026-06-08 No No Current