FDA.reportPublic FDA data

Sensodyne Pronamel

Product NDC
0135-0809
11-digit product format
001350809
Labeler code
0135
Product ID
0135-0809_395866d4-ad69-4f60-8c4c-1c910aba1c38
Type
HUMAN OTC DRUG
Nonproprietary name
sodium fluoride
Dosage form
PASTE
Route
DENTAL
Labeler
Haleon US Holdings LLC
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-06
Substance
SODIUM FLUORIDE
Active strength
1.1 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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
Sensodyne Pronamel
Brand name suffix
Kids Berry Twist
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM FLUORIDE1.1 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8ZYQ1474W7Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
69c07c36-b5e0-420b-ab29-7d1091386322Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0135-0809-01Sensodyne PronamelKids Berry Twist1 in 1 CARTONPASTE12
0135-0809-01Sensodyne PronamelKids Berry Twist113 g in 1 TUBEPASTE1132
0135-0809-02Sensodyne PronamelKids Berry Twist23 g in 1 TUBEPASTE232
0135-0809-03Sensodyne PronamelKids Berry Twist113 g in 1 TUBEPASTE1132
0135-0809-03Sensodyne PronamelKids Berry Twist2 in 1 CARTONPASTE22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0135-0809SENSODYNE PRONAMEL KIDS BERRY TWIST (SODIUM FLUORIDE) PASTE [HALEON US HOLDINGS LLC]1Current NDC, 5 package rows20250107_69c07c36-b5e0-420b-ab29-7d1091386322.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 40 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IoliteBENZOCAINEDharma Research, Inc.e4b2d22b-00b3-45a6-9b7d-8ee7195870592023-10-09WarningsExact identifier
application number: M022
IoliteBENZOCAINEDharma Research, Inc.a0e284f6-292f-4231-8596-f7cee4e0a12f2023-10-09WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLCfe92637a-c88a-f9dd-e053-6294a90a7fa32023-07-01WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLCc979e958-2042-471a-bf03-e84e686201062023-06-20WarningsExact identifier
application number: M022
Orajel Gum Pain 3X MedicatedBENZOCAINE, MENTHOL, ZINC CHLORIDEChurch & Dwight Co., Inc.9a1632ad-2b47-5653-e053-2995a90ae0d92023-01-20WarningsExact identifier
application number: M022
KOLORZ TOPICAL ANESTHETIC TRIPLE MINTBENZOCAINEDMG AMERICA, LLC0f90b227-f938-4e1a-a79e-1967b1a0477e2021-10-01WarningsExact identifier
application number: M022

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0135-0809-01001350809011 TUBE in 1 CARTON (0135-0809-01) / 113 g in 1 TUBE1 tube2025-01-06NoNoCurrent
0135-0809-020013508090223 g in 1 TUBE (0135-0809-02) 23 g2025-01-06NoNoCurrent
0135-0809-03001350809032 TUBE in 1 CARTON (0135-0809-03) / 113 g in 1 TUBE2 tube2026-01-01NoNoCurrent