CTx4 Gel 1100

Product NDC
61578-204
Requested package NDC
61578-204-01
11-digit product format
615780204
Labeler code
61578
Product ID
61578-204_df3e4bdc-62fb-0e6f-e053-2a95a90aa179
Type
HUMAN OTC DRUG
Nonproprietary name
sodium fluoride
Dosage form
GEL, DENTIFRICE
Route
DENTAL
Labeler
Dental Alliance Holdings LLC
Application
part355
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-05-01
Marketing end
0000-00-00
Substance
SODIUM FLUORIDE
Active strength
1100 ug/g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage61578-20461578-204-01DDiscontinued by firm2026-10-05

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 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31DDiscontinued by firm2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28DDiscontinued by firma1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21DDiscontinued by firmcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10DDiscontinued by firmcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31DDiscontinued by firm302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20DDiscontinued by firmed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10DDiscontinued by firm0efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08DDiscontinued by firmad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03DDiscontinued by firm367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09DDiscontinued by firm557ba5c1ecfa…9c80585c8c6e…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…
2021-12-27 23:28 UTC · source 2021-12-27IInactivated by FDA8dfbde2a14a4…c9ff85d89658…
2020-12-18 03:04 UTC · source 2020-12-17IInactivated by FDAe2bbac7714bc…27bdfed8d636…
2020-06-10 20:45 UTC · source 2020-06-10IInactivated by FDA9bebd1f3094a…5416666fcb17…
2019-12-08 06:16 UTC · source 2019-12-05IInactivated by FDA110d247fa046…a55b01930146…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61578-204-012022-05-17C16284748780-19855e2a2-367b-60a7-e053-dbdaa90a05bdGel 1100
61578-204-012019-11-27C16284748780-19855e2a2-367b-60a7-e053-dbdaa90a05bdGel 1100

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W7CTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
FLUORIDE IONACTIVE MOIETYQ80VPU408OCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
HYDRATED SILICAINACTIVE INGREDIENTY6O7T4G8P9CTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
HYDROXYETHYL CELLULOSE (3000 CPS AT 1%)INACTIVE INGREDIENT7Q6P4JN1QTCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
MALTITOLINACTIVE INGREDIENTD65DG142WKCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
MENTHOLINACTIVE INGREDIENTL7T10EIP3ACTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
POLYSORBATE 20INACTIVE INGREDIENT7T1F30V5YHCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
POTASSIUM SORBATEINACTIVE INGREDIENT1VPU26JZZ4CTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
SACCHARININACTIVE INGREDIENTFST467XS7DCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32ICTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
TRIBASIC CALCIUM PHOSPHATEINACTIVE INGREDIENT91D9GV0Z28CTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
WATERINACTIVE INGREDIENT059QF0KO0RCTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1
XYLITOLINACTIVE INGREDIENTVCQ006KQ1ECTX4 GEL 1100 MINT (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 CITRUS (SODIUM FLUORIDE) GEL, DENTIFRICE CTX4 GEL 1100 GRAPE (SODIUM FLUORIDE) GEL, DENTIFRICE [ORAL BIOTECH]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61578-204-016157802040156.699 g in 1 TUBE, WITH APPLICATOR (61578-204-01) 56.699 g2012-05-010000-00-00NoNoCurrent