Home NDC 79481-0008 Sensitive Whitening Tooth-paste
Product NDC 79481-0008
11-digit product format 794810008
Labeler code 79481
Product ID 79481-0008_e9579105-80a5-440e-8da2-b31b65542f32
Type HUMAN OTC DRUG
Nonproprietary name Potassium nitrate, Sodium fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Meijer, Inc.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-24
Substance POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength 50; 2.43 mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 79481-0008-1 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 79481-0008-1 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 79481-0008-1 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 79481-0008-1 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 79481-0008-1 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 79481-0008-1 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 79481-0008-1 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 79481-0008-1 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 79481-0008-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 Sensitive Whitening Tooth-paste
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM NITRATE 50 mg/g SODIUM FLUORIDE 2.43 mg/g
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 1038800 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79481-0008-1 Sensitive Whitening Tooth-paste 113 g in 1 TUBE PASTE, DENTIFRICE 113 4 79481-0008-1 Sensitive Whitening Tooth-paste 1 in 1 BOX PASTE, DENTIFRICE 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79481-0008 SENSITIVE WHITENING TOOTH-PASTE (POTASSIUM NITRATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [MEIJER, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20230112_c25b6a95-e604-48e3-bc55-595969d1ce9b.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 2 of 40 · 786 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tumeez Organic Apple CALCIUM CARBONATE BFY LLC f561685a-5260-59c6-e053-2a95a90ae206 2026-08-25 Warnings Exact identifier application number: M022 Ludens Watermelon Throat Drops PECTIN Prestige Brands Holdings, Inc. adfb248a-96bb-4742-9df6-c47edccdd671 2026-08-20 Warnings Exact identifier application number: M022 Antiseptic EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL WALMART INC. (see also Equate) 584b38ce-d1ef-4ecc-a887-7c96e7f9669f 2026-08-20 Warnings Exact identifier application number: M022 Antiseptic EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL Walgreens fb93c7f6-e025-4cf2-9997-acfe9a0debdd 2026-08-19 Warnings Exact identifier application number: M022 CVS Saline NASAL CVS PHARMACY f02c41b0-c78e-41cd-aa4a-2756bbe92087 2026-08-19 Warnings Exact identifier application number: M022 Listerine UltraClean Gum Plus Whitening Protection Cool Mint Antigingivitis/ Antiplaque Mouthwash EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL Kenvue Brands LLC 5965eb2a-1261-5258-e063-6294a90a7c2d 2026-08-19 Warnings Exact identifier application number: M022 Ludens Honey Licorice Throat Drops MENTHOL Prestige Brands Holdings, Inc. 5dc2baec-a9ed-4f6b-a7ed-76a5d35739ac 2026-08-19 Warnings Exact identifier application number: M022 Ludens Dual Relief PECTIN AND MENTHOL Prestige Brands Holdings, Inc. d0213cb3-ec8e-40cc-82c9-694032f0490f 2026-08-19 Warnings Exact identifier application number: M022 CVS Health Sore Throat Fast Relief Oral Anesthetic PHENOL CVS Pharmacy,Inc. 4fb880db-2185-41ef-a5f9-8983a28d2c5b 2026-08-17 Warnings Exact identifier application number: M022 CVS Sore Throat Cherry PHENOL CVS Pharmacy,Inc. 887c68e0-ff44-4bad-b360-56fb99ed9c45 2026-08-17 Warnings Exact identifier application number: M022 CVS Sore Throat Menthol Flavor PHENOL CVS PHARMACY,INC. 665be058-b965-4b78-80b0-dd8524180932 2026-08-17 Warnings Exact identifier application number: M022 Hydrogen Peroxide 3 Percent HYDROGEN PEROXIDE Harris Teeter, LLC 7e5f175d-f0d6-4665-ac14-1873d6b99c80 2026-08-12 Warnings Exact identifier application number: M022 Gingicaine Gel Variety Pak GINGICAINE GEL VARIETY PAK Gingi-Pak a Division of the Belport 62ed4ff3-18f6-5c67-e053-2991aa0a7792 2026-08-11 Warnings Exact identifier application number: M022 Hydrogen Peroxide 3 Percent ReadyInCase HYDROGEN PEROXIDE P & L Development, LLC b0866db5-3b0d-4478-9b3b-1f077d2f5393 2026-08-06 Warnings Exact identifier application number: M022 Ollie Fresh Mint SODIUM FLUORIDE, POTASSIUM NITRATE Brio Product Group LLC. ebeec44f-3c22-43f2-9256-6ece6025c105 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 5868c5a1-273f-f023-e063-6394a90ac9d8 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 58690bb5-9604-26a4-e063-6394a90afdbe 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 586918cf-7b13-5999-e063-6294a90a88a9 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 586924a0-322d-5dc3-e063-6294a90a1556 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 58692e90-de74-52d3-e063-6394a90a9702 2026-08-06 Warnings Exact identifier application number: M022
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 79481-0008-1 79481000801 1 TUBE in 1 BOX (79481-0008-1) / 113 g in 1 TUBE 1 tube 2020-12-24 0000-00-00 No No Current