Home NDC 42509-134 United Dental Kit
Product NDC 42509-134
11-digit product format 425090134
Labeler code 42509
Product ID 42509-134_08aaf4ce-9b3c-5491-e063-6294a90a8a4e
Type HUMAN OTC DRUG
Nonproprietary name SODIUM MONOFLUOROPHOSPHATE
Dosage form KIT
Labeler Wessco International
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-06-01
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 United Dental Kit
Listing expiration 2026-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 545626 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 42509-134-01 United Dental Kit 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 42509-134 UNITED DENTAL KIT (SODIUM MONOFLUOROPHOSPHATE) KIT [WESSCO INTERNATIONAL] 2 Current NDC, 1 package rows 20231027_7f348fe7-9918-4934-bed0-f0a77c09d046.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 38 of 49 · 974 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 42509-134-01 42509013401 1 KIT in 1 KIT (42509-134-01) * 5 g in 1 TUBE (42555-060-94) 1 kit 2023-06-01 No No Current