Home NDC 11822-0213-4 Anticavity
Product NDC 11822-0213
Requested package NDC 11822-0213-4
11-digit product format 118220213
Labeler code 11822
Product ID 11822-0213_63bab830-063c-4a91-aca0-0a689195395f
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride
Dosage form RINSE
Route ORAL
Labeler Rite Aid
Application part355
Marketing category OTC MONOGRAPH FINAL
Marketing start 2005-02-25
Marketing end 0000-00-00
Substance SODIUM FLUORIDE
Active strength 0 mg/mL
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 11822-0213 11822-0213-4 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-0213 ANTICAVITY (SODIUM FLUORIDE) RINSE [RITE AID] 22 Legacy NDC 20250406_217f8129-1cdf-41ee-99a2-3de4dd3c82c7.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11822-0213-4 11822021304 532 mL in 1 BOTTLE, PLASTIC (11822-0213-4) 532 ml 2005-02-25 0000-00-00 No No Current