TARGET UP AND UP ANTICAVITY

Product NDC
82442-106
11-digit product format
824420106
Labeler code
82442
Product ID
82442-106_40ab0ae2-4f73-e0d4-e063-6394a90a9b43
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM FLUORIDE 0.05%
Dosage form
MOUTHWASH
Route
ORAL
Labeler
TARGET CORPORATION
Application
M021
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-12-18
Substance
SODIUM FLUORIDE
Active strength
.05 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data

Finished product
Yes
Brand name base
TARGET UP AND UP ANTICAVITY
Listing expiration
2026-12-31

Related Records

Active Ingredients

IngredientStrength
SODIUM FLUORIDE.05 g/100mL

Harmonized Identifiers

FieldValues
Unii8ZYQ1474W7
Rxcui240698

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
8ZYQ1474W7SODIUM FLUORIDE7681-49-4SODIUM FLUORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82442-106-1682442010616473 mL in 1 BOTTLE (82442-106-16) 473 ml2024-12-18NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
TARGET UP & UP ANTICAVITY ORAL RINSETARGET CORPORATION2025-10-08HUMAN OTC DRUG LABEL2