PCXX 1.64 STANNOUS RNSSTRAWBERRY

Product NDC
62007-302
11-digit product format
620070302
Labeler code
62007
Product ID
62007-302_8afdf7b5-833a-4cab-964c-497bc94e674a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FLUORIDE TREATMENT
Dosage form
LIQUID
Route
TOPICAL
Labeler
Ross Healthcare Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2015-01-01
Marketing end
0000-00-00
Substance
STANNOUS FLUORIDE
Active strength
16 1/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
62007-302-642020-01-31C16284748780-19d75b9cf-d68b-f424-e053-dadaa90a57ce737bbdcb-489a-4711-843d-e1b721c2c952

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62007-302-64PCXX 1.64 STANNOUS RNSSTRAWBERRY1 mg in 1 BOTTLE, PLASTICLIQUID11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62007-302PCXX 1.64 STANNOUS RNSSTRAWBERRY (FLUORIDE TREATMENT) LIQUID [ROSS HEALTHCARE INC.]1Legacy NDC, 1 package rows20150203_737bbdcb-489a-4711-843d-e1b721c2c952.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
62007-302-64620070302641 mg in 1 BOTTLE, PLASTIC1 mgHistorical