FDA.reportPublic FDA data

Kiss My Face

Manufacturer
Kiss My Face, LLC | Lornamead Inc.
Effective date
2019-02-20
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 Triple Action
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure10 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Sodium Monofluorphosphate 0.15% w/w fluoride ion

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 under 6 years of age.
  • 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 Glycerin, Aqua, Hydrated Silica, Sorbitol, Xylitol, Calcium Carbonate, Olea Europaea (Olive) Leaf Extract, Cetraria Islandica (Iceland Moss) Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Stevia Rebaudiana Extract, Natural Flavor, Xanthan Gum, Sodium Methyl Cocoyl Taurate, Sodium Lauroyl Sarcosinate, Titanium Dioxide, Zinc Citrate, Potassium Sorbate

SPL UNCLASSIFIED SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KISS MY FACE®

BREATH BLASTING FRESHNESS™

TRIPLE ACTION ANTICAVITY FLUORIDE Toothpaste with Xylitol

REMOVES PLAQUE • WHITENS • PREVENTS TARTAR BUILD-UP

Fresh Mint Paste

Great Taste - No Triclosan/SLS

antioxidant defenders™: tea tree oil • olive leaf extract

Net Wt.. 4.1 oz (116.2 g)

KMF 65363-402 Triple Action Anticavity Toothpaste Fresh MintKMF 65363-402 Triple Action Anticavity Toothpaste Fresh 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
65364-402-162020-09-27C16284748780-1ab0e2407-3322-f274-e053-dbdaa90a6471Kiss My Face Triple Action Toothpaste Fresh Mint
65364-402-162020-09-25C16284748780-1ab0e2407-3322-f274-e053-dbdaa90a6471Kiss My Face Triple Action Toothpaste Fresh Mint
65364-402-162020-07-22C16284748780-1ab0e2407-3322-f274-e053-dbdaa90a6471Kiss My Face Triple Action Toothpaste Fresh Mint

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65364-402-16Kiss My FaceTriple Action1 in 1 CARTONPASTE, DENTIFRICE11
65364-402-16Kiss My FaceTriple Action116.2 g in 1 TUBEPASTE, DENTIFRICE116.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65364-402KISS MY FACE TRIPLE ACTION (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [KISS MY FACE, LLC]1Legacy NDC, 2 package rows20190220_82537fd4-c879-bb38-e053-2a91aa0a30ac.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65364-40265364-402-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
SORBITOL506T60A25RIACT
WATER059QF0KO0RIACT
TEA TREE OILVIF565UC2GIACT
OLEA EUROPAEA LEAFMJ95C3OH47IACT
SODIUM METHYL COCOYL TAURATEJVL98CG53GIACT
SODIUM MONOFLUOROPHOSPHATEC810JCZ56QACTIM
SODIUM LAUROYL SARCOSINATE632GS99618IACT
XANTHAN GUMTTV12P4NEEIACT
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT
CETRARIA ISLANDICA SUBSP. ISLANDICABJ7YPN79A1IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
GLYCERINPDC6A3C0OXIACT
HYDRATED SILICAY6O7T4G8P9IACT
XYLITOLVCQ006KQ1EIACT
CALCIUM CARBONATEH0G9379FGKIACT
ZINC CITRATEK72I3DEX9BIACT
TITANIUM DIOXIDE15FIX9V2JPIACT

Source Document#

Source XML · Source PDF

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
82537fd4-c878-bb38-e053-2a91aa0a30ac82537fd4-c879-bb38-e053-2a91aa0a30ac2019-02-20WarningsExact identifier
spl id: 82537fd4-c878-bb38-e053-2a91aa0a30ac
spl set id: 82537fd4-c879-bb38-e053-2a91aa0a30ac

Reported adverse events (FAERS/openFDA)#

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