Salivea

Manufacturer
Laclede, Inc.
Effective date
2026-02-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:44:15

Label at a glance#

ProductSalivea
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure10 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 a day, or as directed by a dentist or doctor. To minimize swallowing for children under 6, use a pea-size amount and supervise brushing until good habits are established. Children under 2 years ask a dentist or physician.

Storage and handling

Store at Room Temperature.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Sodium Monofluorophosphate (0.14% w/v fluoride ion)

PURPOSE

OTC - PURPOSE SECTION

Anticavity

USES

INDICATIONS & USAGE SECTION

Aids in the prevention of dental cavities.

WARNINGS

WARNINGS SECTION

Keep out of the reach of children under 6 years of age.

If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children under 6 years of age.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.
  • To minimize swallowing for children under 6, use a pea-size amount and supervise brushing until good habits are established. Children under 2 years ask a dentist or physician.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store at Room Temperature.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sorbitol, Glycerin, Calcium Pyrophosphate, Water, Hydrated Silica, Xylitol, Silica, Hydroxyethylcellulose, Isoceteth-20, Cellulose Gum, Flavor, Sodium Benzoate, Lactoperoxidase, Potassium Thiocyanate, Glucose Oxidase, Lysozyme, Lactoferrin, Dextranase, Calcium Lactate.

QUESTIONS

OTC - QUESTIONS SECTION

Questions? Comments? Call toll-free: 1-877-522-5333

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SALIVEA DRY MOUTH CARE TOOTHPASTE

Soothing Mint

with Xylitol & Calcium

image of cartonimage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
851054sodium monofluorophosphate 0.14 % ToothpastePSN1
851054sodium monofluorophosphate 0.0014 MG/MG ToothpasteSCD1
851054sodium monofluorophosphate 0.14 % Dental GelSY1
851054sodium monofluorophosphate 0.14 % ToothpasteSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54897-701-14Salivea21 g in 1 TUBEPASTE, DENTIFRICE211

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54897-70154897-701-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SaliveaFLUORIDE TOOTHPASTELaclede, Inc.4abb0f80-d87d-730f-e063-6294a90a15f72026-02-13WarningsExact identifier
ndc (package): 54897-701-14
ndc (product): 54897-701
ndc11 (package): 54897070114
spl id: 4abb0c37-6135-135b-e063-6394a90a38b2
spl set id: 4abb0f80-d87d-730f-e063-6294a90a15f7
SaliveaFLUORIDE TOOTHPASTELaclede, Inc.6398ae96-dd38-44da-bc34-1d4d4c4a78ca2025-01-08WarningsExact identifier
ndc (product): 54897-701

Reported adverse events (FAERS/openFDA)#

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