Plus White

Product NDC
61543-1751
Requested package NDC
61543-1751-3
11-digit product format
615431751
Labeler code
61543
Product ID
61543-1751_af060a95-bec3-4f9c-85c6-e98454637efb
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM MONOFLUOROPHOSPHATE
Dosage form
PASTE, DENTIFRICE
Route
ORAL
Labeler
CCA Industries, Inc.
Application
part355
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2018-05-22
Substance
SODIUM MONOFLUOROPHOSPHATE
Active strength
.83 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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
Plus White
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM MONOFLUOROPHOSPHATE.83 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
C810JCZ56QInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1247591Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
7581b27b-6acb-45b0-8804-b5dae3498931Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61543-1751-3Plus White56.6 g in 1 TUBEPASTE, DENTIFRICE56.61
61543-1751-3Plus White1 in 1 CARTONPASTE, DENTIFRICE11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61543-1751PLUS WHITE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [CCA INDUSTRIES, INC.]1Current NDC, Legacy NDC, 2 package rows20180807_7581b27b-6acb-45b0-8804-b5dae3498931.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Plus WhiteSODIUM MONOFLUOROPHOSPHATECCA Industries, Inc.7581b27b-6acb-45b0-8804-b5dae34989312018-08-01WarningsExact identifier
ndc (package): 61543-1751-3
ndc (product): 61543-1751
ndc11 (package): 61543175103

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1247591sodium monofluorophosphate 0.83 % (fluoride 0.11 % ) ToothpastePSN7581b27b-6acb-45b0-8804-b5dae34989311
1247591sodium monofluorophosphate 0.0083 MG/MG ToothpasteSCD7581b27b-6acb-45b0-8804-b5dae34989311
1247591sodium monofluorophosphate 0.83 % ToothpasteSY7581b27b-6acb-45b0-8804-b5dae34989311

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61543-1751-3615431751031 TUBE in 1 CARTON (61543-1751-3) / 56.6 g in 1 TUBE1 tube2018-05-220000-00-00NoNoCurrent