Home NDC 59088-630 Naprotin
Product NDC 59088-630
11-digit product format 590880630
Labeler code 59088
Product ID 59088-630_292f7fd5-53b4-9da9-e063-6394a90a52e6
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Naproxen , Capsaicin
Dosage form KIT
Route ORAL
Labeler PureTek Corporation
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-09-27
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 Naprotin
Listing expiration 2026-12-31
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198014 Internal RxNorm lookup 198555 Internal RxNorm 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 50228-436-01 Naprotin 100 in 1 BOTTLE TABLET 100 500 mg 2 59088-630-00 Naprotin 1 in 1 KIT KIT 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59088-630 NAPROTIN (NAPROXEN , CAPSAICIN) KIT [PURETEK CORPORATION] 2 Current NDC, Legacy NDC, 2 package rows 20241215_dc2d2783-2a73-cb7c-e053-2995a90a9961.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 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Naprotin NAPROXEN , CAPSAICIN PureTek Corporation dc2d2783-2a73-cb7c-e053-2995a90a9961 2024-12-13 Boxed warning, Warnings, Adverse reactions Exact identifier ndc (product): 59088-630
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50228-436-01 50228043601 100 in 1 BOTTLE Historical 59088-630-00 59088063000 1 KIT in 1 KIT (59088-630-00) * 100 TABLET in 1 BOTTLE (50228-436-01) * 237 mL in 1 BOTTLE, PUMP (59088-310-16) 1 kit 2022-09-27 0000-00-00 No No Current