Home NDC 69396-175 Pain Relief
Product NDC 69396-175
11-digit product format 693960175
Labeler code 69396
Product ID 69396-175_54a12a51-5caa-b953-e063-6294a90ac4d4
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form SPRAY
Route TOPICAL
Labeler Trifecta Pharmaceuticals USA, LLC.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-25
Substance MENTHOL
Active strength 10.5 g/100mL
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 Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 10.5 g/100mL
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 1489073 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 69396-175-03 Pain Relief 89 mL in 1 BOTTLE, SPRAY SPRAY 89 5
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 48 of 153 · 3,057 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 69396-175-03 69396017503 89 mL in 1 BOTTLE, SPRAY (69396-175-03) 89 ml 2026-01-25 No No Current