PCXX PEPPERMINT APF F

Product NDC
62007-059
11-digit product format
620070059
Labeler code
62007
Product ID
62007-059_3a777df2-0ece-8799-e063-6294a90a3105
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
AEROSOL, FOAM
Route
DENTAL; TOPICAL
Labeler
Ross Healthcare Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-11-21
Substance
SODIUM FLUORIDE
Active strength
.0272 g/g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
PCXX PEPPERMINT APF F
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM FLUORIDE.0272 g/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii8ZYQ1474W7
Rxcui248389

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62007-059-07PCXX PEPPERMINT APF F125 g in 1 CANAEROSOL, FOAM1256

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62007-059PCXX PEPPERMINT APF F (SODIUM FLUORIDE) AEROSOL, FOAM [ROSS HEALTHCARE INC.]5Current NDC, Legacy NDC, 1 package rows20250214_5e86783c-414a-5f46-e053-2991aa0abb3b.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
248389sodium fluoride 2.72 % Oral FoamPSN5e86783c-414a-5f46-e053-2991aa0abb3b6
248389sodium fluoride 27.2 MG/ML Oral FoamSCD5e86783c-414a-5f46-e053-2991aa0abb3b6
248389sodium fluoride 2.72 % (fluoride ion 1.23 % ) Oral FoamSY5e86783c-414a-5f46-e053-2991aa0abb3b6
248389sodium fluoride 2.72 % Oral FoamSY5e86783c-414a-5f46-e053-2991aa0abb3b6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62007-059-0762007005907125 g in 1 CAN (62007-059-07) 125 g2017-11-210000-00-00NoNoCurrent