Home NDC 63404-0201 SprinJene
Product NDC 63404-0201
11-digit product format 634040201
Labeler code 63404
Product ID 63404-0201_d02d031a-f428-4114-b5f3-8a518ffc08cf
Type HUMAN OTC DRUG
Nonproprietary name Sodium Monofluorophosphate
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Health and Natural Beauty USA Corp
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-02-01
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength 1.5 mg/g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 44 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 63404-0201-1 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 63404-0201-1 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 63404-0201-1 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 63404-0201-1 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 63404-0201-1 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 63404-0201-1 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 63404-0201-1 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 63404-0201-1 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 63404-0201-1 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 63404-0201-1 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 63404-0201-1 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 63404-0201-1 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 63404-0201-1 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 63404-0201-1 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 63404-0201-1 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 63404-0201-1 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 63404-0201-1 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 63404-0201-1 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 63404-0201-1 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 63404-0201-1 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 63404-0201-1 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 63404-0201-1 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base SprinJene
Brand name suffix Natural
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM MONOFLUOROPHOSPHATE 1.5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C810JCZ56Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 545626 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63404-0201-1 SprinJene Natural 99 g in 1 TUBE PASTE, DENTIFRICE 99 1 63404-0201-1 SprinJene Natural 1 in 1 CARTON PASTE, DENTIFRICE 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63404-0201 SPRINJENE NATURAL (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [HEALTH AND NATURAL BEAUTY USA CORP] 1 Current NDC, Legacy NDC, 2 package rows 20170201_e64cecc3-0845-4bdf-a449-d78248791ccf.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 3 of 51 · 1,013 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SprinJene Fresh Boost SODIUM FLUORIDE Health and Natural Beauty USA Corp 919f6f51-6c43-4f1c-9bc7-029bf76c0e68 2026-08-14 Warnings Exact identifier application number: M021 SprinJene Natural Sensitivity Relief SODIUM MONOFLUOROPHOSPHATE AND POTASSIUM NITRATE Health and Natural Beauty USA Corp 32cc5bc2-60c9-4cb4-acde-485ae494aba2 2026-08-14 Warnings Exact identifier application number: M021 SprinJene White Boost SODIUM FLUORIDE Health and Natural Beauty USA Corp 8c401bea-0148-46a0-bbb3-80c17f9e8e3e 2026-08-14 Warnings Exact identifier application number: M021 ULTRA BRITE Baking Soda and Peroxide Whitening Cool Mint SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive Company 2b123d70-4f7d-41b0-b48f-711999e97ee0 2026-08-13 Warnings Exact identifier application number: M021 COLGATE STRAWBERRY BURST SODIUM FLUORIDE Colgate-Palmolive Company d037f65c-3d22-4d2a-a0a9-3dcba2357ebd 2026-08-13 Warnings Exact identifier application number: M021 COLGATE OPTIC WHITE PRO SERIES ENAMEL RENEWAL SOOTHING MINT SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive Company cd954777-697a-4cc7-8f5f-b2caf357ef95 2026-08-13 Warnings Exact identifier application number: M021 TOMS OF MAINE KIDS SILLY STRAWBERRY SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. e36ceb7a-9a29-41d8-8d08-a859e515f1f5 2026-08-13 Warnings Exact identifier application number: M021 TOMS OF MAINE WHOLE CARE SPEARMINT SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 08d7ed04-67a4-437a-82c5-496f9893c6c7 2026-08-10 Warnings Exact identifier application number: M021 TOMS OF MAINE WICKED FRESH COOL PEPPERMINT SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 27278b02-c4fd-4092-a632-a14e442f5a95 2026-08-10 Warnings Exact identifier application number: M021 TOMS OF MAINE WICKED FRESH SPEARMINT ICE SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 59a6b9ac-c28b-4ec3-8231-f35054ce0eaf 2026-08-10 Warnings Exact identifier application number: M021 Toms Kids Watermelon Wiggle SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 48eaafb6-99f4-5fd1-10fc-4ea35cbb2c62 2026-08-10 Warnings Exact identifier application number: M021 AutoBrush kids bubblegum SODIUM FLUORIDE Lander Enterprises, LLC 64b60e74-fceb-4de9-a966-73bf8dbd666c 2026-08-10 Warnings Exact identifier application number: M021 AutoBrush kids strawberry SODIUM FLUORIDE Lander Enterprises, LLC 7e880d50-8aab-4d57-abc1-e900070f9a11 2026-08-10 Warnings Exact identifier application number: M021 AutoBrush kids watermelon SODIUM FLUORIDE Lander Enterprises, LLC 5cb5eb46-705c-4bb7-bef1-e93a598636fd 2026-08-10 Warnings Exact identifier application number: M021 AutoBrush Mint SODIUM FLUORIDE Lander Enterprises, LLC 0e043431-9d87-478d-87f5-5aa8b0a932eb 2026-08-10 Warnings Exact identifier application number: M021 Willo Minty Mist Dye Free SODIUM FLUORIDE Willo 32, Inc. 3ee5b49e-ca9a-ece6-e063-6394a90a3d00 2026-08-10 Warnings Exact identifier application number: M021 Willo Bubble Twist SODIUM FLUORIDE Willo 32 Inc 36560d62-e901-1f93-e063-6394a90a2803 2026-08-10 Warnings Exact identifier application number: M021 Willo Berry Splash Dye Free SODIUM FLUORIDE Willo 32, Inc 3ea91af9-2895-e530-e063-6394a90a39e5 2026-08-10 Warnings Exact identifier application number: M021 Fluoride Mouth Rinse Anticavity SODIUM FLUORIDE Target Corporation 3daf3cc3-585a-4bb2-9b56-7117d220ed38 2026-08-10 Warnings, Adverse reactions Exact identifier application number: M021 TOMS OF MAINE KIDS OUTRAGEOUS ORANGE MANGO SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 19de1e71-ab94-415f-b66d-e5748dea8317 2026-08-10 Warnings Exact identifier application number: M021
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 63404-0201-1 63404020101 1 TUBE in 1 CARTON (63404-0201-1) / 99 g in 1 TUBE 1 tube 2017-02-01 No No Current