PCXX VANILLA ORANGE NEUTRAL F

Product NDC
62007-101
11-digit product format
620070101
Labeler code
62007
Product ID
62007-101_ba3dceee-9ed4-d2b8-e053-2995a90ac03b
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
Marketing end
0000-00-00
Substance
SODIUM FLUORIDE
Active strength
0 g/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62007-101-072021-01-31C16284748780-1ba0f9c33-24c7-a910-e053-dadaa90a0b85PCXX VANILLA ORANGE NEUTRAL F
62007-101-072021-01-29C16284748780-1ba0f9c33-24c7-a910-e053-dadaa90a0b85PCXX VANILLA ORANGE NEUTRAL F

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62007-101PCXX VANILLA ORANGE NEUTRAL F (SODIUM FLUORIDE) AEROSOL, FOAM [ROSS HEALTHCARE INC.]6Legacy NDC20250201_5e87ca30-ebc2-3498-e053-2991aa0abac9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62007-101-0762007010107125 g in 1 CAN (62007-101-07) 125 g2017-11-210000-00-00NoNoCurrent