SELAHATIN

Manufacturer
Selahatin AB
Effective date
2022-07-17
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:56:41

Label at a glance#

ProductSELAHATIN ALL VARIANTS
Active ingredientSODIUM FLUORIDE
Label structure9 sections

Indications and uses

Aids in the prevention of dental caries (decay)

Dosage and administration

1) Use once or twice a day after brushing your teeth 2) Rinse in closed mouth for 30-60 seconds 3) Spit out. Don’t swallow. Do not eat or drink for 30 minutes after use. This mouthwash is not a substitute for your regular dental hygien

Storage and handling

Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Sodium Flouride........1100ppm

PURPOSE

OTC - PURPOSE SECTION

Anti-caries

USES

INDICATIONS & USAGE SECTION

  • Aids in the prevention of dental caries (decay)

WARNINGS

WARNINGS SECTION

Do not rinse mouth with water afterwards. The mouthwash does not replace the regular tooth hygiene routine.

Do not:

  • Use in case of a known hypersensitivity or allergy to any of the ingredients.
  • Use in association with other mouthwash products.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

1) Use once or twice a day after brushing your teeth 2) Rinse in closed mouth for 30-60 seconds 3) Spit out. Don’t swallow.

Do not eat or drink for 30 minutes after use.

This mouthwash is not a substitute for your regular dental hygien

OTHER INFORMATION

STORAGE AND HANDLING SECTION

  • Protect this product from excessive heat and direct sun.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ESCAPIST: Aqua/[Water], Glycerin, Pvp, Polysorbate 20, Propylene Glycol, Poloxamer 407, PEG-40 Hydrogenated Castor Oil, Sodium Citrate, Aroma/[Flavor], Potassium Sorbate, Sodium Benzoate, Sodium Phosphate, Tocopheryl Acetate, Disodium Phosphate, Panthenol, Limonene, Aloe Barbadensis Leaf Juice Powder, Bisabolol, Cetylpyridinium Chloride, Sodium Saccharin, BHT

ELISE: Aqua/[Water], Glycerin, Pvp, Polysorbate 20, Propylene Glycol, Poloxamer 407, PEG-40 Hydrogenated Castor Oil, Sodium Citrate, Potassium Sorbate, Sodium Benzoate, Limonene, Sodium Phosphate, Aroma/[Flavor], Tocopheryl Acetate, Menthyl Ethylamido Oxalate, Disodium Phosphate, Panthenol, Aloe Barbadensis Leaf Juice Powder, Bisabolol, Cetylpyridinium Chloride, Sodium Saccharin, Citrus Limon Peel Oil/[Citrus Limon (Lemon) Peel Oil], Eucalyptus Globulus Leaf Oil, Citrus Aurantifolia Oil/[Citrus Aurantifolia (Lime) Oil], Citral, BHT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL (PDP)_Mouthwash_Elise_200mL01b LBL (PDP)_Mouthwash_Elise_200mL

01b LBL (DF Box)_Mouthwash_Elise_200mL01b LBL (DF Box)_Mouthwash_Elise_200mL

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80130-10280130-102-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

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
e792e252-8d87-dcde-e053-2a95a90a436ecae0c7a0-8aca-177e-e053-2a95a90a78e72022-08-31WarningsExact identifier
spl set id: cae0c7a0-8aca-177e-e053-2a95a90a78e7

Reported adverse events (FAERS/openFDA)#

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