Home NDC 82711-002-01 Lab52 Anti-Sensitivity Oral Care
Product NDC 82711-002
Requested package NDC 82711-002-01
11-digit product format 827110002
Labeler code 82711
Product ID 82711-002_de6312fd-1a5d-ba2a-e053-2a95a90ae0c2
Type HUMAN OTC DRUG
Nonproprietary name XYLITOL, CALCIUM LACTATE, POTASSIUM CITRATE
Dosage form AEROSOL
Route DENTAL
Labeler TOOTHFILM INC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-05-07
Marketing end 0000-00-00
Substance CALCIUM LACTATE; POTASSIUM CITRATE; XYLITOL
Active strength 0 g/100g; g/100g; g/100g
Pharmacologic classes Acidifying Activity [MoA], Anti-coagulant [EPC], Blood Coagulation Factor [EPC], Calcium Chelating Activity [MoA], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Decreased Coagulation Factor Activity [PE], 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 · 12 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 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…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…
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 82711-002-01 82711000201 15 g in 1 BOTTLE, SPRAY (82711-002-01) 15 g 2022-05-07 0000-00-00 No No Current