ADVANCED FLUORIDE ANTICAVITY

Product NDC
29500-9181
11-digit product format
295009181
Labeler code
29500
Product ID
29500-9181_3113d887-5ed1-4aa3-8725-913db8c3dfba
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM MONOFLUOROPHOSPHATE
Dosage form
PASTE, DENTIFRICE
Route
DENTAL
Labeler
Personal Care Products, LLC
Application
part355
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-07-24
Marketing end
0000-00-00
Substance
SODIUM MONOFLUOROPHOSPHATE
Active strength
1000 mg/181g
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
29500-9181-62020-01-31C16284748780-19d75b9d0-b7e2-f424-e053-dadaa90a57ceADVANCED FLUORIDE ANTICAVITY TOOTHPASTE - 9181

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
29500-9181-6ADVANCED FLUORIDE ANTICAVITY181 g in 1 TUBEPASTE, DENTIFRICE1811
29500-9181-6ADVANCED FLUORIDE ANTICAVITY1 in 1 PACKAGEPASTE, DENTIFRICE11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
29500-9181ADVANCED FLUORIDE ANTICAVITY (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [PERSONAL CARE PRODUCTS, LLC]1Legacy NDC, 2 package rows20170801_7881ff17-5188-47e6-8d2b-9c296ce35411.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
29500-9181-629500918106181 g in 1 TUBE181 gHistorical