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

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 Identifiers#

Field, Values table
FieldValues
Unii8ZYQ1474W7

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

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 tube2025-01-06NoNoHistorical
0135-0809-020013508090223 g in 1 TUBE (0135-0809-02) 23 g2025-01-06NoNoHistorical
0135-0809-03001350809032 TUBE in 1 CARTON (0135-0809-03) / 113 g in 1 TUBE2 tube2026-01-01NoNoHistorical