PCXX APF RNS MINT

Product NDC
62007-311
11-digit product format
620070311
Labeler code
62007
Product ID
62007-311_a3d0a044-7e31-4b3a-b967-707b618d3819
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FLUORIDE TREATMENT
Dosage form
LIQUID
Route
TOPICAL
Labeler
Ross Healthcare Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2015-02-02
Marketing end
0000-00-00
Substance
SODIUM FLUORIDE
Active strength
27 mg/mg
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62007-311-642020-01-31C16284748780-19d75b9cf-d68e-f424-e053-dadaa90a57ce55dd20c9-94f5-4b3a-be81-64a1eeb1ed26

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62007-311-64PCXX APF RNS MINT1 mg in 1 BOTTLE, PLASTICLIQUID11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W7PCXX APF RNS MINT (FLUORIDE TREATMENT) LIQUID [ROSS HEALTHCARE INC.]1
FLUORIDE IONACTIVE MOIETYQ80VPU408OPCXX APF RNS MINT (FLUORIDE TREATMENT) LIQUID [ROSS HEALTHCARE INC.]1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDPCXX APF RNS MINT (FLUORIDE TREATMENT) LIQUID [ROSS HEALTHCARE INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62007-311PCXX APF RNS MINT (FLUORIDE TREATMENT) LIQUID [ROSS HEALTHCARE INC.]1Legacy NDC, 1 package rows20150203_55dd20c9-94f5-4b3a-be81-64a1eeb1ed26.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
62007-311-64620070311641 mg in 1 BOTTLE, PLASTIC1 mgHistorical