Orajel Sensitivity Relief

Product NDC
10237-678
11-digit product format
102370678
Labeler code
10237
Product ID
10237-678_88d71cb7-8abf-407d-a74c-f5537497759a
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Fluoride and Potassium Nitrate
Dosage form
PASTE, DENTIFRICE
Route
ORAL
Labeler
Church & Dwight Co., Inc.
Application
M021
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-01-31
Substance
POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength
5; .243 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Orajel Sensitivity Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POTASSIUM NITRATE5 g/100g
SODIUM FLUORIDE.243 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiRU45X2JN0Z, 8ZYQ1474W7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10237-678-12Orajel Sensitivity Relief2 in 1 CARTONPASTE, DENTIFRICE22
10237-678-12Orajel Sensitivity Relief170 g in 1 TUBEPASTE, DENTIFRICE1702
10237-678-43Orajel Sensitivity Relief121.9 g in 1 TUBEPASTE, DENTIFRICE121.92

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10237-678ORAJEL SENSITIVITY RELIEF (SODIUM FLUORIDE AND POTASSIUM NITRATE) PASTE, DENTIFRICE [CHURCH & DWIGHT CO., INC.]2Current NDC, 3 package rows20240404_7b9d9e7d-3844-4d18-ab03-bd0e9dcfccdb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
10237-678-12102370678122 TUBE in 1 CARTON (10237-678-12) / 170 g in 1 TUBE2 tube2024-06-01NoNoCurrent
10237-678-4310237067843121.9 g in 1 TUBE (10237-678-43) 121.9 g2024-01-31NoNoCurrent