Bad Breath Killer

Product NDC
79717-0011
11-digit product format
797170011
Labeler code
79717
Product ID
79717-0011_ce40bf79-1b0a-4995-aaaf-94a8f721db46
Type
HUMAN OTC DRUG
Nonproprietary name
Propolis
Dosage form
STRIP
Route
DENTAL
Labeler
TECOZYME INC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2021-08-01
Marketing end
0000-00-00
Substance
PROPOLIS WAX
Active strength
8 mg/100mg
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
79717-0011-22022-07-29C16284748780-1e4f33bdf-9f77-d8a0-e053-dadaa90a6e4e18390af7-0faa-498f-89e3-1fea263aaf2d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79717-0011-1Bad Breath Killer84.5 mg in 1 POUCHSTRIP84.51
79717-0011-2Bad Breath Killer14 in 1 CARTONSTRIP141

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79717-0011BAD BREATH KILLER (PROPOLIS) STRIP [TECOZYME INC]1Legacy NDC, 2 package rows20210818_18390af7-0faa-498f-89e3-1fea263aaf2d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79717-0011-17971700110184.5 mg in 1 POUCH84.5 mgHistorical
79717-0011-27971700110214 POUCH in 1 CARTON (79717-0011-2) > 84.5 mg in 1 POUCH (79717-0011-1) 14 pouch2021-08-010000-00-00NoNoCurrent