Home NDC 74724-0031-1 SALTRAIN LTOOTHPASTE
Product NDC 74724-0031
Requested package NDC 74724-0031-1
11-digit product format 747240031
Labeler code 74724
Product ID 74724-0031_f126e30f-5f3a-7bf9-e053-2a95a90a265d
Type HUMAN OTC DRUG
Nonproprietary name sodium chloride, Precipitated Calcium Carbonate
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler K.Boeun Pharmaceutical Co.,Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2023-01-01
Marketing end 0000-00-00
Substance CALCIUM CARBONATE; SODIUM CHLORIDE
Active strength 33 g/100g; g/100g
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 74724-0031-1 SALTRAIN LTOOTHPASTE 180 g in 1 TUBE PASTE, DENTIFRICE 180 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 74724-0031 SALTRAIN LTOOTHPASTE (SODIUM CHLORIDE, PRECIPITATED CALCIUM CARBONATE) PASTE, DENTIFRICE [K.BOEUN PHARMACEUTICAL CO.,LTD.] 1 Legacy NDC, 1 package rows 20230101_f126df43-b31a-13c2-e053-2a95a90a523c.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 74724-0031-1 74724003101 180 g in 1 TUBE (74724-0031-1) 180 g 2023-01-01 0000-00-00 No No Current