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 43 of 50 · 995 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Listerine Total Care Zero Alcohol Anticavity Fresh Mint SODIUM FLUORIDE Kenvue Brands LLC 4b594a6e-db1d-443b-bfa7-23ee15749f47 2024-12-19 Warnings Exact identifier application number: M021 NewYork-Presbyterian Amenity SODIUM MONOFLUOROPHOSPATE ASP Global, LLc 4b307471-445d-4c51-a499-d074a8172f20 2024-12-17 Warnings Exact identifier application number: M021 Colgate Anticavity SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive (Thailand) Limited - Branch 5bc0b430-6f68-4e52-a1da-de19136eaeac 2024-12-09 Warnings Exact identifier application number: M021 CURODONT REPAIR FLUORIDE PLUS SODIUM FLUORIDE CREDENTIS AG 03ec09f9-4281-9ccb-e063-6294a90aadd8 2024-12-01 Warnings Exact identifier application number: M021 CURODONT PROTECT STANNOUS FLUORIDE CREDENTIS AG 03ec591c-68c3-a380-e063-6394a90a131a 2024-12-01 Warnings Exact identifier application number: M021 ACT Kids Anticavity Fluoride Bubble Gum Blowout SODIUM FLUORIDE Chattem, Inc. 61f3a3e6-645b-4368-b1d5-7de1fc14542e 2024-12-01 Warnings Exact identifier application number: M021 SparkleFresh Flouride Toothpaste SODIUM MONOFLUOROPHOSPHATE Medline Industries, LP 1565528b-89f2-4c97-b294-15b6ebd3f80e 2024-11-26 Warnings Exact identifier application number: M021 Rembrandt Intense Stain SODIUM FLUORIDE Ranir LLC 55dcd063-5661-35aa-e054-00144ff8d46c 2024-11-26 Warnings Exact identifier application number: M021 Firefly Anticavity Fluoride SODIUM FLUORIDE Ranir LLC 9f98913f-6754-4e1c-98cf-b89fe87750f8 2024-11-25 Warnings Exact identifier application number: M021 Colgate Total SF Clean Mint STANNOUS FLUORIDE Colgate-Palmolive Company 88f87f7a-5b2d-47c9-8830-6b88b4ddbb59 2024-11-25 Warnings Exact identifier application number: M021 Firefly Bubble Gum natural fluoride SODIUM FLUORIDE Ranir LLC 0c85d273-3b98-43ea-81ba-c90f70ab72f8 2024-11-25 Warnings Exact identifier application number: M021 Firefly Bubble Gum natural fluoride SODIUM FLUORIDE Ranir LLC 2a882210-49e6-4b9c-a2c6-eaa37b6514c3 2024-11-25 Warnings Exact identifier application number: M021 Pepsodent Complete Care Original SODIUM FLUORIDE Church & Dwight Co., Inc. 3c6931cb-0ec9-41bb-b410-c355573aab57 2024-11-21 Warnings Exact identifier application number: M021 Firefly Strawberry Natural Fluoride SODIUM FLUORIDE Ranir LLC 8ee37955-fe1a-4964-ac29-d1d7dfb694cc 2024-11-21 Warnings Exact identifier application number: M021 Firefly Anticavity Fluoride SODIUM FLUORIDE Ranir LLC abdc7f79-5f87-4307-8ddd-e6281ac67a04 2024-11-20 Warnings Exact identifier application number: M021 AIM Bubble Berry SODIUM FLUORIDE Church & Dwight Co., Inc. c83ccdea-d75f-4084-853e-ed4bab9a12d4 2024-11-20 Warnings Exact identifier application number: M021 AIM TARTAR CONTROL Plus Mouthwash and Whitening SODIUM FLUORIDE Church & Dwight Co., Inc. 1d0fc71c-d28e-4afa-e054-00144ff8d46c 2024-11-20 Warnings Exact identifier application number: M021 Advance White Tartar Control Breath Freshening SODIUM FLUORIDE Church & Dwight Co., Inc. aa8be8f5-ba46-4b1b-afaa-58fddf8f8780 2024-11-20 Warnings Exact identifier application number: M021 Enamel Defense SODIUM FLUORIDE Church & Dwight Co., Inc. 9e8f1ce9-b161-50db-e053-2995a90ad32b 2024-11-20 Warnings Exact identifier application number: M021 Rembrandt Deeply White Plus Peroxide SODIUM MONOFLUOROPHOSPHATE Ranir LLC bf7da007-ab9d-4631-bc28-6ca245fd6265 2024-11-20 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