Home NDC 69204-005 Pain Release
Product NDC 69204-005
11-digit product format 692040005
Labeler code 69204
Product ID 69204-005_471f5c2f-0e22-8065-e063-6394a90a1be4
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form GRANULE
Route TOPICAL
Labeler Natures Formulae Health Products Ltd.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-10-16
Substance MENTHOL
Active strength 1.6 mg/g
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 Pain Release
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 1.6 mg/g
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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69204-005-06 Pain Release 620 g in 1 BOTTLE, PLASTIC GRANULE 620 2 69204-005-07 Pain Release 1 in 1 PACKET GRANULE 1 2 69204-005-07 Pain Release 120 g in 1 POUCH GRANULE 120 2 69204-005-08 Pain Release 300 g in 1 BOTTLE, PLASTIC GRANULE 300 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69204-005 PAIN RELEASE (MENTHOL) GRANULE [NATURES FORMULAE HEALTH PRODUCTS LTD.] 1 Current NDC, Legacy NDC, 4 package rows 20181014_781d3c8d-7b70-e973-e053-2991aa0aaa78.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69204-005-06 69204000506 620 g in 1 BOTTLE, PLASTIC (69204-005-06) 620 g 2016-10-16 0000-00-00 No No Current 69204-005-07 69204000507 1 POUCH in 1 PACKET (69204-005-07) / 120 g in 1 POUCH 1 pouch 2016-10-16 0000-00-00 No No Current 69204-005-08 69204000508 300 g in 1 BOTTLE, PLASTIC (69204-005-08) 300 g 2025-12-12 No No Current