FDA.reportPublic FDA data

Kiss My Face

Manufacturer
Kiss My Face, LLC | Lornamead Inc.
Effective date
2019-02-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:58:35

Label at a glance#

ProductKiss My Face Whitening
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure10 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Sodium monofluorphosphate 0.76% w/w

OTC - PURPOSE SECTION

Purpose

Anticavity

INDICATIONS & USAGE SECTION

Uses

Aids in the prevention of

  • dental cavities
  • plaque and tartar build-up

WARNINGS SECTION

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.
  • If you accidentally swallow more than used for brushing, contact a Poison Control Center or seek professional assistance immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply at least a 1 inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day or as recommended by a dentist or doctor.
  • Children under 6 years of age: consult a dentist or doctor

OTHER SAFETY INFORMATION

Other information

You may report a serious adverse event from using this product to Kiss My Face, LLC, 144 Main Street, Gardiner, NY 12525.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Sorbitol, Glycerin, Hydrated Silica, Aqua, Xylitol, Aloe Barbadensis (Aloe Vera) Leaf Extract*, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Olea Europaea (Olive) Leaf Extract, Cetraria Islandica (Iceland Moss) Extract, Stevia Rebaudiana Extract, Natural Flavor, Mentha Piperita (Peppermint) Oil, Menthol, Ammonium Glycyrrhizate (Licorice), Xanthan Gum, Cellulose Gum, Sodium Methyl Cocoyl Taurate, Sodium Lauroyl Sarcosinate, Chlorophyllin-Copper Complex, Potassium Sorbate

*Organic

SPL UNCLASSIFIED SECTION

Dist. Kiss My Face LLC, Gardiner, NY 12525 USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KISS MY FACE®

BREATH BLASTING FRESHNESS™

WHITENING ANTICAVITY FLUORIDE Toothpaste with Xylitol

WHITENS • REMOVES PLAQUE

Cool Mint Gel

Great Taste - No Triclosan/SLS

antioxidant defenders™: Iceland moss extract • tea tree oil

Net Wt. 4.5 oz (127.6 g)

KMF 65364-400 Anticavity Whitening Gel Cool MintKMF 65364-400 Anticavity Whitening Gel Cool Mint

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
545626sodium monofluorophosphate 0.76 % ToothpastePSN1
545626sodium monofluorophosphate 0.0076 MG/MG ToothpasteSCD1
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )ToothpasteSY1
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )ToothpasteSY1
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )ToothpasteSY1
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.15 % )ToothpasteSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65364-400-272020-09-27C16284748780-1ab0e2407-2acd-f274-e053-dbdaa90a6471Kiss My Face Whitening Toothpaste
65364-400-272020-09-25C16284748780-1ab0e2407-2acd-f274-e053-dbdaa90a6471Kiss My Face Whitening Toothpaste
65364-400-272020-07-22C16284748780-1ab0e2407-2acd-f274-e053-dbdaa90a6471Kiss My Face Whitening Toothpaste

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65364-400-27Kiss My FaceWhitening1 in 1 CARTONGEL, DENTIFRICE11
65364-400-27Kiss My FaceWhitening127.6 g in 1 TUBEGEL, DENTIFRICE127.61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65364-400KISS MY FACE WHITENING (SODIUM MONOFLUOROPHOSPHATE) GEL, DENTIFRICE [KISS MY FACE, LLC]1Legacy NDC, 2 package rows20190220_822ce0f7-b8a6-6a5d-e053-2991aa0a11fb.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65364-40065364-400-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEPPERMINT OILAV092KU4JHIACT
SORBITOL506T60A25RIACT
WATER059QF0KO0RIACT
TEA TREE OILVIF565UC2GIACT
OLEA EUROPAEA LEAFMJ95C3OH47IACT
SODIUM METHYL COCOYL TAURATEJVL98CG53GIACT
SODIUM MONOFLUOROPHOSPHATEC810JCZ56QACTIM
SODIUM LAUROYL SARCOSINATE632GS99618IACT
AMMONIUM GLYCYRRHIZATE3VRD35U26CIACT
XANTHAN GUMTTV12P4NEEIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORMK679OBS311IACT
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT
MENTHOLL7T10EIP3AIACT
CETRARIA ISLANDICA SUBSP. ISLANDICABJ7YPN79A1IACT
SODIUM COPPER CHLOROPHYLLIN1D276TYV9OIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
GLYCERINPDC6A3C0OXIACT
HYDRATED SILICAY6O7T4G8P9IACT
XYLITOLVCQ006KQ1EIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
822ce0f7-b8a7-6a5d-e053-2991aa0a11fb822ce0f7-b8a6-6a5d-e053-2991aa0a11fb2019-02-18WarningsExact identifier
spl id: 822ce0f7-b8a7-6a5d-e053-2991aa0a11fb
spl set id: 822ce0f7-b8a6-6a5d-e053-2991aa0a11fb

Reported adverse events (FAERS/openFDA)#

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