Home NDC 71141-187 dentalux SENSITIVE ANTI-CAVITY FLUORIDE
Product NDC 71141-187
11-digit product format 711410187
Labeler code 71141
Product ID 71141-187_fc734f34-1c0f-4211-b5aa-bbd0ba55d821
Type HUMAN OTC DRUG
Nonproprietary name Potassium Nitrate, Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Lidl US, LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-06-30
Substance POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength 5; .24 g/100g; g/100g
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 dentalux SENSITIVE ANTI-CAVITY FLUORIDE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM NITRATE 5 g/100g SODIUM FLUORIDE .24 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination RU45X2JN0Z Internal UNII lookup 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1038929 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 71141-187-10 dentalux SENSITIVE ANTI-CAVITY FLUORIDE 1 in 1 BOX PASTE, DENTIFRICE 1 1 71141-187-10 dentalux SENSITIVE ANTI-CAVITY FLUORIDE 113 g in 1 TUBE PASTE, DENTIFRICE 113 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71141-187 DENTALUX SENSITIVE ANTI-CAVITY FLUORIDE (POTASSIUM NITRATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [LIDL US, LLC] 1 Current NDC, 2 package rows 20241121_baef7f15-8082-4e61-8c08-8beda8ad40c0.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 9 of 40 · 786 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 71141-187-10 71141018710 1 TUBE in 1 BOX (71141-187-10) / 113 g in 1 TUBE 1 tube 2024-06-30 No No Current