Home NDC 70602-010-02 EXODEN ALL IN ONE
Product NDC 70602-010
Requested package NDC 70602-010-02
11-digit product format 706020010
Labeler code 70602
Product ID 70602-010_e3b4a328-f6e8-7aaf-e053-2a95a90a5ab5
Type HUMAN OTC DRUG
Nonproprietary name Silicon dioxide, Tetrasodium Pyrophosphate, Sodium Monofluorophosphate, sodium fluoride
Dosage form PASTE
Route TOPICAL
Labeler LIFEON Corp.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-07-13
Marketing end 0000-00-00
Substance SILICON DIOXIDE; SODIUM FLUORIDE; SODIUM MONOFLUOROPHOSPHATE; SODIUM PYROPHOSPHATE
Active strength 10 g/100g; g/100g; g/100g; g/100g
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70602-010-01 EXODEN ALL IN ONE 100 g in 1 TUBE PASTE 100 1 70602-010-02 EXODEN ALL IN ONE 1 in 1 CARTON PASTE 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70602-010 EXODEN ALL IN ONE (SILICON DIOXIDE, TETRASODIUM PYROPHOSPHATE, SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE) PASTE [LIFEON CORP.] 1 Legacy NDC, 2 package rows 20220715_e69fcf60-39f8-46ff-99c1-b78872fd72f0.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70602-010-02 70602001002 1 TUBE in 1 CARTON (70602-010-02) > 100 g in 1 TUBE (70602-010-01) 1 tube 2022-07-13 0000-00-00 No No Current