evo SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT

Product NDC
70108-254
11-digit product format
701080254
Labeler code
70108
Product ID
70108-254_bb2a34f2-d5a9-4335-bd5b-e8dbc231657b
Type
HUMAN OTC DRUG
Nonproprietary name
Potassium Nitrate, Sodium Fluoride
Dosage form
PASTE, DENTIFRICE
Route
DENTAL
Labeler
Ashtel Studios, Inc.
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-10-01
Substance
POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength
5; .24 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
evo SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT
Listing expiration
2026-12-31

Related Records

Active Ingredients

IngredientStrength
POTASSIUM NITRATE5 g/100g
SODIUM FLUORIDE.24 g/100g

Harmonized Identifiers

FieldValues
UniiRU45X2JN0Z, 8ZYQ1474W7
Rxcui1038929

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
RU45X2JN0ZPOTASSIUM NITRATE7757-79-1POTASSIUM NITRATE
8ZYQ1474W7SODIUM FLUORIDE7681-49-4SODIUM FLUORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70108-254-01701080254011 TUBE in 1 BOX (70108-254-01) / 99 g in 1 TUBE1 tube2025-10-01NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
evo ® SENSITIVE ANTI-CAVITY FLUORIDE TOOTHPASTE SWEET MINTAshtel Studios, Inc.2025-10-13HUMAN OTC DRUG LABEL1