Home NDC 67510-0111 Mint
Product NDC 67510-0111
11-digit product format 675100111
Labeler code 67510
Product ID 67510-0111_9db6552e-e4ae-3c5e-e053-2a95a90a50cf
Type HUMAN OTC DRUG
Nonproprietary name Sodium Monofluorophosphate
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Kareway Product, Inc.
Application part355
Marketing category OTC MONOGRAPH FINAL
Marketing start 2011-08-15
Marketing end 0000-00-00
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength 1 g/100g
NDC exclude flag No
Listing certified through 2021-12-31
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 67510-0111-4 fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 67510-0111-6 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 67510-0111-4 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 67510-0111-6 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 67510-0111-4 bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 67510-0111-6 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 67510-0111-4 67510011104 1 TUBE in 1 BOX (67510-0111-4) > 181 g in 1 TUBE 1 tube 2011-08-15 0000-00-00 No No Current 67510-0111-6 67510011106 1 TUBE in 1 BOX (67510-0111-6) > 170 g in 1 TUBE 1 tube 2011-08-15 0000-00-00 No No Current