FDA.reportPublic FDA data

AP-24 Whitening

Manufacturer
NSE Products, Inc.
Effective date
2026-03-24
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:51:23

Label at a glance#

ProductAP-24 Whitening
Active ingredientSodium Monofluorophosphate
Label structure9 sections

Indications and uses

Aids in the prevention of dental cavities.

Dosage and administration

Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice daily, or as directed by a dentist or doctor for optimal cavity prevention. Instruct children under 6 years of age on good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 2 years of age: Consult a dentist ...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Sodium Monofluorophosphate (0.76%)

Purpose

OTC - PURPOSE SECTION

anticavity

Uses

INDICATIONS & USAGE SECTION

  • Aids in the prevention of dental cavities.

Warning

WARNINGS SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children under 6 years of age. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice daily, or as directed by a dentist or doctor for optimal cavity prevention.
  • Instruct children under 6 years of age on good brushing and rinsing habits (to minimize swallowing).
  • Supervise children as necessary until capable of using without supervision.
  • Children under 2 years of age: Consult a dentist or doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Hydrated Silica, Sorbitol, Aluminum Hydroxide, Glycerin, Tetrasodium Pyrophosphate, Poloxamer 338, PEG-12, Poloxamer 407, Dimethicone, Cellulose Gum, Sodium Lauryl Sulfate, Flavor (Aroma), Sodium Saccharin, Titanium Dioxide (CI 77891)

Questions?

OTC - QUESTIONS SECTION

1-801-345-9900

PRINCIPAL DISPLAY PANEL - 110 g Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NU SKIN®

AP 24®
Whitening
Fluoride
Toothpaste

110 g ℮ Net Wt. 3.9 Oz

PRINCIPAL DISPLAY PANEL - 110 g Tube Label
PRINCIPAL DISPLAY PANEL - 110 g Tube Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
545626sodium monofluorophosphate 0.76 % ToothpastePSN5
545626sodium monofluorophosphate 0.0076 MG/MG ToothpasteSCD5
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )ToothpasteSY5
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )ToothpasteSY5
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )ToothpasteSY5
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.15 % )ToothpasteSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62839-1155-1AP-24 Whitening110 g in 1 TUBEPASTE1105

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62839-115562839-1155-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
Sodium MonofluorophosphateC810JCZ56QACTIM
Water059QF0KO0RIACT
Hydrated SilicaY6O7T4G8P9IACT
Sorbitol506T60A25RIACT
Aluminum Hydroxide5QB0T2IUN0IACT
GlycerinPDC6A3C0OXIACT
Sodium PyrophosphateO352864B8ZIACT
Polyethylene Glycol 600NL4J9F21N9IACT
Dimethicone92RU3N3Y1OIACT
Poloxamer 338F75JV2T505IACT
Poloxamer 407TUF2IVW3M2IACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311IACT
Sodium Lauryl Sulfate368GB5141JIACT
Saccharin SodiumSB8ZUX40TYIACT
Titanium Dioxide15FIX9V2JPIACT

Source Document#

Source XML

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
AP-24 WhiteningSODIUM MONOFLUOROPHOSPHATENSE Products, Inc.57e9e68c-41dd-470b-80db-dfaedc0e2a0a2026-03-24WarningsExact identifier
ndc (package): 62839-1155-1
ndc (product): 62839-1155
ndc11 (package): 62839115501
spl id: 1621e578-4a1f-4dbe-8cf7-1fce4b978cb3
spl set id: 57e9e68c-41dd-470b-80db-dfaedc0e2a0a

Reported adverse events (FAERS/openFDA)#

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