Sensodyne Pronamel

Product NDC
0135-0808
11-digit product format
001350808
Labeler code
0135
Product ID
0135-0808_1f91320f-d81f-d5ef-e063-6394a90ad72d
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 Bubble 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
0135-0808-01Sensodyne PronamelKids Bubble Twist113 g in 1 TUBEPASTE1131
0135-0808-01Sensodyne PronamelKids Bubble Twist1 in 1 CARTONPASTE11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0135-0808SENSODYNE PRONAMEL KIDS BUBBLE TWIST (SODIUM FLUORIDE) PASTE [HALEON US HOLDINGS LLC]1Current NDC, 2 package rows20250107_e403529a-0fac-4dab-b75c-46906add096b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0135-0808-01001350808011 TUBE in 1 CARTON (0135-0808-01) / 113 g in 1 TUBE1 tube2025-01-06NoNoCurrent