Home NDC 70983-010 Pain Release
Product NDC 70983-010
11-digit product format 709830010
Labeler code 70983
Product ID 70983-010_48514309-b4d2-69e9-e063-6294a90afe9e
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form KIT
Labeler Saje Natural Business Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-10-16
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 Release
Listing expiration 2027-12-31 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 70983-010-12 Pain Release 1 in 1 KIT KIT 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70983-010 PAIN RELEASE (MENTHOL) KIT [SAJE NATURAL BUSINESS INC.] 4 Current NDC, Legacy NDC, 1 package rows 20231007_481a493b-0620-46ac-8228-e9964b7eb24b.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 108 of 152 · 3,029 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 70983-010-12 70983001012 1 KIT in 1 KIT (70983-010-12) * 10 mL in 1 BOTTLE, DROPPER * 40 mL in 1 BOTTLE, DROPPER * 30 mL in 1 BOTTLE, SPRAY * 1 POUCH in 1 PACKAGE / 120 g in 1 POUCH 1 kit 2016-10-16 0000-00-00 No No Current