Home NDC 69261-005-03 Quip Anticavity Fluoride
Product NDC 69261-005
Requested package NDC 69261-005-03
11-digit product format 692610005
Labeler code 69261
Product ID 69261-005_2cefad39-aaec-e49b-e063-6394a90adc9d
Type HUMAN OTC DRUG
Nonproprietary name SODIUM FLUORIDE
Dosage form MOUTHWASH
Route DENTAL
Labeler Quip NYC Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-25
Substance SODIUM FLUORIDE
Active strength .05 g/100mL
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
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 Quip Anticavity Fluoride
Brand name suffix Concentrate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .05 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 240698 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 69261-005-03 Quip Anticavity FluorideConcentrate 117.5 mL in 1 BOTTLE MOUTHWASH 117.5 3 69261-005-04 Quip Anticavity FluorideConcentrate 1 in 1 CARTON MOUTHWASH 1 3 69261-005-04 Quip Anticavity FluorideConcentrate 117.5 mL in 1 BOTTLE MOUTHWASH 117.5 3 69261-005-05 Quip Anticavity FluorideConcentrate 117.5 mL in 1 BOTTLE MOUTHWASH 117.5 3 69261-005-05 Quip Anticavity FluorideConcentrate 1 in 1 PACKAGE MOUTHWASH 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69261-005 QUIP ANTICAVITY FLUORIDE CONCENTRATE (SODIUM FLUORIDE) MOUTHWASH [QUIP NYC INC.] 3 Current NDC, Legacy NDC, 5 package rows 20250201_b3da65bb-0871-34e7-e053-2a95a90a310e.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 4 of 50 · 995 matching rows.
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 69261-005-03 69261000503 117.5 mL in 1 BOTTLE (69261-005-03) 117.5 ml 2021-01-25 0000-00-00 No No Current