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
2
Source
full-release
Hydrated at
2026-05-31 22:58:35

Label at a glance#

ProductKiss My Face Sensitive
Active ingredientPOTASSIUM NITRATE
Label structure10 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Potassium Nitrate 5.0% w/w

OTC - PURPOSE SECTION

Purpose

Tooth desensitizer

INDICATIONS & USAGE SECTION

Uses

Helps relieve sensitivity of the teeth to cold, heat, acids or sweet.

Aids in the prevention of plaque and tarter build-up.

WARNINGS SECTION

Warnings

  • Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. See your dentist if the problem persists or worsens.

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 one minute, preferably after each meal or at least 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 St, Gardiner NY 12525.

INACTIVE INGREDIENT SECTION

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

*Organic

SPL UNCLASSIFIED SECTION

Dist: Kiss My Face LLC

Gardiner, NY 12525 USA

Made in USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KISS MY FACE

BREATH BLASTING FRESHNESS

SENSITIVE

FLUORIDE FREE Natural Aloe Toothpaste with Xylitol

Orange Mint Gel

HELPS REDUCE SENSITIVITY • PREVENTS TARTAR BUILD-UP

antioxidant defenders™: echinacea • Iceland moss extract

NET WT 4.5 OZ (127.6 g)

KMF 65364-401 Sensitive Fluoride Free ToothpasteKMF 65364-401 Sensitive Fluoride Free Toothpaste

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312544potassium nitrate 5 % ToothpastePSN2
312544potassium nitrate 0.05 MG/MG ToothpasteSCD2
312544K+ nitrate 0.05 MG/MG ToothpasteSY2
312544Pot nitrate 0.05 MG/MG ToothpasteSY2
312544potassium nitrate 5 % ToothpasteSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65364-401-272020-09-27C16284748780-1ab0e2407-2ad0-f274-e053-dbdaa90a6471Kiss My Face Sensitive Fluoride Free
65364-401-272020-09-25C16284748780-1ab0e2407-2ad0-f274-e053-dbdaa90a6471Kiss My Face Sensitive Fluoride Free
65364-401-272020-07-22C16284748780-1ab0e2407-2ad0-f274-e053-dbdaa90a6471Kiss My Face Sensitive Fluoride Free

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65364-401-27Kiss My FaceSensitive1 in 1 CARTONGEL, DENTIFRICE12
65364-401-27Kiss My FaceSensitive127.6 g in 1 TUBEGEL, DENTIFRICE127.62

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65364-401KISS MY FACE SENSITIVE (POTASSIUM NITRATE) GEL, DENTIFRICE [KISS MY FACE, LLC]2Legacy NDC, 2 package rows20190220_825303be-4043-467f-e053-2a91aa0af692.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65364-40165364-401-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETRARIA ISLANDICA SUBSP. ISLANDICABJ7YPN79A1IACT
SODIUM LAURYL SARCOSINATE5PGH842FAUIACT
SORBITOL506T60A25RIACT
AESCULUS HIPPOCASTANUM SEED OILE0M52HIR1YIACT
TEA TREE OILVIF565UC2GIACT
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
HYDRATED SILICAY6O7T4G8P9IACT
OLEA EUROPAEA LEAFMJ95C3OH47IACT
SODIUM METHYL COCOYL TAURATEJVL98CG53GIACT
ALOE VERA LEAFZY81Z83H0XIACT
POTASSIUM NITRATERU45X2JN0ZACTIB
ECHINACEA ANGUSTIFOLIA LEAFFS7G8S6PJ8IACT
MENTHOLL7T10EIP3AIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
XYLITOLVCQ006KQ1EIACT
SODIUM COPPER CHLOROPHYLLIN1D276TYV9OIACT
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT
MENTHA PIPERITA79M2M2UDA9IACT
AMMONIUM GLYCYRRHIZATE3VRD35U26CIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORMK679OBS311IACT

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
825303be-4035-467f-e053-2a91aa0af692825303be-4043-467f-e053-2a91aa0af6922019-02-20WarningsExact identifier
spl id: 825303be-4035-467f-e053-2a91aa0af692
spl set id: 825303be-4043-467f-e053-2a91aa0af692

Reported adverse events (FAERS/openFDA)#

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