Home NDC 85410-050 Mantra Pain Gel raspberry
Product NDC 85410-050
11-digit product format 854100050
Labeler code 85410
Product ID 85410-050_584f5a99-35fb-2dd9-e063-6394a90aae50
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form GEL
Route ORAL
Labeler MOREMED INC.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-17
Substance ACETAMINOPHEN
Active strength .5 g/24g
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 Mantra Pain Gel raspberry
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN .5 g/24g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D 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 1 of 83 · 1,657 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85410-050-02 85410005002 24 g in 1 POUCH (85410-050-02) 24 g 2025-11-17 No No Current