PCXX STRAWBERRY APF G

Product NDC
62007-810
11-digit product format
620070810
Labeler code
62007
Product ID
62007-810_ba3dc6df-55d3-8ad1-e053-2a95a90a71b0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
GEL
Route
DENTAL; TOPICAL
Labeler
Ross Healthcare Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-02-04
Marketing end
0000-00-00
Substance
SODIUM FLUORIDE
Active strength
27 mg/mL
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
62007-810-162021-01-31C16284748780-1ba0f9c33-1021-a910-e053-dadaa90a0b85PCXX STRAWBERRY APF GEL
62007-810-162021-01-29C16284748780-1ba0f9c33-1021-a910-e053-dadaa90a0b85PCXX STRAWBERRY APF GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62007-810-16PCXX STRAWBERRY APF G473 mL in 1 BOTTLE, PLASTICGEL4735

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62007-810PCXX STRAWBERRY APF G (SODIUM FLUORIDE) GEL [ROSS HEALTHCARE INC.]5Legacy NDC, 1 package rows20250201_828026cc-ea66-7b3d-e053-2a91aa0a7588.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1535362sodium fluoride 2.72 % Oral GelPSN828026cc-ea66-7b3d-e053-2a91aa0a75885
1535362sodium fluoride 0.0272 MG/MG Oral GelSCD828026cc-ea66-7b3d-e053-2a91aa0a75885
1535362sodium fluoride 2.72 % (fluoride ion 1.23 % ) Oral GelSY828026cc-ea66-7b3d-e053-2a91aa0a75885

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62007-810-1662007081016473 mL in 1 BOTTLE, PLASTIC (62007-810-16) 473 ml2019-02-040000-00-00NoNoCurrent