FDA.reportPublic FDA data

Kroger

Product NDC
30142-149
11-digit product format
301420149
Labeler code
30142
Product ID
30142-149_4dc6c0d2-89b4-999e-e063-6394a90a2ed7
Type
HUMAN OTC DRUG
Nonproprietary name
Fluoride
Dosage form
PASTE, DENTIFRICE
Route
DENTAL
Labeler
Kroger
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2011-01-20
Substance
SODIUM FLUORIDE; POTASSIUM NITRATE
Active strength
.15; 5 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage30142-14930142-149-89DDiscontinued by firm2026-10-16

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Kroger
Brand name suffix
Extra Whitening
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM FLUORIDE.15 g/100g
POTASSIUM NITRATE5 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8ZYQ1474W7Internal UNII lookup
RU45X2JN0ZInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1038929Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
e704c690-1383-4cd6-be85-28bdd9ff936bAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30142-149-89KrogerExtra Whitening1 in 1 CAPSULEPASTE, DENTIFRICE119
30142-149-89KrogerExtra Whitening226 g in 1 TUBEPASTE, DENTIFRICE22619
30142-149-92KrogerExtra Whitening113 g in 1 TUBEPASTE, DENTIFRICE11319
30142-149-99KrogerExtra Whitening1 in 1 CARTONPASTE, DENTIFRICE119

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
POTASSIUM NITRATEACTIVE INGREDIENTRU45X2JN0ZKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W7KROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
FLUORIDE IONACTIVE MOIETYQ80VPU408OKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
NITRATE IONACTIVE MOIETYT93E9Y2844KROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
COCAMIDOPROPYL BETAINEINACTIVE INGREDIENT5OCF3O11KXKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
HYDRATED SILICAINACTIVE INGREDIENTY6O7T4G8P9KROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TYKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32IKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
SODIUM METHYL COCOYL TAURATEINACTIVE INGREDIENTJVL98CG53GKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
SODIUM TRIPOLYPHOSPHATEINACTIVE INGREDIENT5HK03SA80JKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
SORBITOLINACTIVE INGREDIENT506T60A25RKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
WATERINACTIVE INGREDIENT059QF0KO0RKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1
XANTHAN GUMINACTIVE INGREDIENTTTV12P4NEEKROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-149KROGER EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [KROGER]14Current NDC, Legacy NDC, 4 package rows20250312_e704c690-1383-4cd6-be85-28bdd9ff936b.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 16 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GuruNanda OxyfusionHYDROGEN PEROXIDEGURUNANDA, LLC3be317b9-a5d8-b198-e063-6394a90af9852025-11-11WarningsExact identifier
application number: M022
GuruNanda Oral Pain ReliefMENTHOLGURUNANDA, LLC3b8f3562-0e46-bea4-e063-6294a90adb712025-11-11WarningsExact identifier
application number: M022
TopCare Cherry FlavorPHENOLTOPCO ASSOCIATES, LLC5d3f0610-deb4-4180-ae19-2c65ed2f368b2025-11-10WarningsExact identifier
application number: M022
Topcare Sore Throat Menthol FlavorPHENOLTOPCO ASSOCIATES LLCfb1f2c11-2508-4985-bae5-7d547bd6aa232025-11-10WarningsExact identifier
application number: M022
Zilactin-BBENZOCAINEASCENT CONSUMER PRODUCTS, INC42eeb3d4-bac6-4e29-e063-6294a90a644d2025-11-06WarningsExact identifier
application number: M022
Zilactin Early Relief Cold SoreBENZYL ALCOHOLASCENT CONSUMER PRODUCTS, INC42ef8bfa-c4d9-01cf-e063-6394a90ac88a2025-11-06WarningsExact identifier
application number: M022
HurriCaine Topical Anesthetic GelBENZOCAINEBeutlich Pharmaceuticals, LLC106b6115-d043-4050-80c6-1d82456dea022025-11-06WarningsExact identifier
application number: M022
HurriCaine Topical Anesthetic GelBENZOCAINEBeutlich Pharmaceuticals, LLC4c278122-2643-46bf-9e44-11985210a16e2025-11-06WarningsExact identifier
application number: M022
HurriCaine Topical Anesthetic LiquidBENZOCAINEBeutlich Pharmaceuticals, LLCfee9969d-ad1a-4f44-9741-a0a44c9e11282025-11-06WarningsExact identifier
application number: M022
Ear Wax Removal Aid DropsCARBAMIDE PEROXIDETarget Corporation0ddf9945-147d-4b25-98a6-4e9f12a4656f2025-11-05WarningsExact identifier
application number: M022
Alpha-Caine Topical AnestheticBENZOCAINEDental Technologies, Inc.e6a312e5-17ac-46f0-8723-4e40eeecd69f2025-11-04WarningsExact identifier
application number: M022
PEROXY SHIELD MOUTH SORE1.5% HYDROGEN PEROXIDEDental Technologies, Inc.a72e433b-1b7d-4a0c-e053-2995a90a30c42025-11-04WarningsExact identifier
application number: M022
Alpha-Caine Topical AnestheticBENZOCAINEDental Technologies, Inc.ae628766-25b7-4b4f-abb8-a43faf2f44b92025-11-04WarningsExact identifier
application number: M022
Alpha-Caine Topical AnestheticBENZOCAINEDental Technologies, Inc.719743f9-21fc-4568-b879-acdfa46394642025-11-04WarningsExact identifier
application number: M022
Alpha-Caine Topical AnestheticBENZOCAINEDental Technologies, Inc.ff0695a1-1d7d-4b51-97fd-689e56d914fe2025-11-04WarningsExact identifier
application number: M022
AntisepticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLFamily Dollar (FAMILY WELLNESS)f7edf75c-cdba-4dde-bfc5-a04af34759d32025-11-03WarningsExact identifier
application number: M022
7 Select Oral Pain Maximum Strength ReliefBENZOCAINE7-ELEVEN, INC.f170a570-1c50-4b9a-be16-9b01bf5eaa742025-10-31WarningsExact identifier
application number: M022
Oral Pain ReliefBENZOCAINE AND BENZALKONIUM CHLORIDEUniversal Distribution Center LLC18520f9b-4d35-1e9c-e063-6294a90aaa392025-10-30WarningsExact identifier
application number: M022
Iodent Oral AnalgesicBENZOCAINEUnited Exchange Corp.63902125-f8dc-0ada-e053-2991aa0a7ce52025-10-30WarningsExact identifier
application number: M022
Ear Wax Removal Aid DropsCARBAMIDE PEROXIDEBETTER LIVING BRANDS, LLC3bded237-4d2c-4b38-bedc-267fdc3741942025-10-29WarningsExact identifier
application number: M022

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1038929potassium nitrate 5 % / sodium fluoride 0.24 % ToothpastePSNe704c690-1383-4cd6-be85-28bdd9ff936b19
1038929potassium nitrate 0.05 MG/MG / sodium fluoride 0.0024 MG/MG ToothpasteSCDe704c690-1383-4cd6-be85-28bdd9ff936b19
1038929K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG ToothpasteSYe704c690-1383-4cd6-be85-28bdd9ff936b19
1038929Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG ToothpasteSYe704c690-1383-4cd6-be85-28bdd9ff936b19
1038929potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.14 % ) ToothpasteSYe704c690-1383-4cd6-be85-28bdd9ff936b19
1038929potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.15 % ) ToothpasteSYe704c690-1383-4cd6-be85-28bdd9ff936b19
1038929potassium nitrate 5 % / sodium fluoride 0.24 % ToothpasteSYe704c690-1383-4cd6-be85-28bdd9ff936b19

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-149-89301420149891 in 1 CAPSULEHistorical
30142-149-9230142014992113 g in 1 TUBE113 gHistorical
30142-149-99301420149991 TUBE in 1 CARTON (30142-149-99) / 113 g in 1 TUBE (30142-149-92) 1 tube2012-11-050000-00-00NoNoCurrent