Seavue Dental Desensitizer

Manufacturer
Xiling (Zhenjiang) Medical Technology Co., Ltd.
Effective date
2025-09-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:38:05

Label at a glance#

ProductSeavue Dental Desensitizer
Active ingredientSODIUM FLUORIDE, POTASSIUM NITRATE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Potassium nitrate, Sodium fluoride

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation, swelling, or allergic reaction occurs.

OTC - DO NOT USE SECTION

Do not use in children under 12 years of age unless recommended by a dentist or physician

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If more than used for treatment is accidentally swallowed, get medical help or contact a Poison Control Center right away.

OTC - PURPOSE SECTION

Oral antiseptic

OTC - WHEN USING SECTION

Use once or twice daily as needed.

DOSAGE & ADMINISTRATION SECTION

Dosage:

Potassium nitrate 2.6% ................................................ Tooth desensitizer
Sodium fluoride 0.3% (0.14% w/v fluoride ion) ............ Anticavity

Use:

Builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact
Aids in the prevention of dental cavities

WARNINGS SECTION

Do not use in children under 12 years of age unless recommended by a dentist or physician
Stop use and ask a dentist if the problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care.
Keep out of reach of children. If more than used for treatment is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Patients with gingival ulcers, stomatitis, or oral mucosal ulcers should use with caution.

INACTIVE INGREDIENT SECTION

None

INDICATIONS & USAGE SECTION

Adults and children 12 years and older:

Apply the product using one of the following methods:

Apply evenly on a mouthguard, wear for 15–30 minutes, then remove and rinse.
Or apply directly to sensitive teeth using a cotton swab or soft brush. Rub gently, leave for 2–3 minutes, rinse and spit out.

Use once or twice daily as needed.

Children under 12 years: ask a dentist.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

123123

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87118-003-01Seavue Dental Desensitizer1 g in 1 BOXGEL, DENTIFRICE11

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87118-00387118-003-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SODIUM FLUORIDE8ZYQ1474W7ACTIM
POTASSIUM NITRATERU45X2JN0ZACTIB

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
Seavue Dental DesensitizerPOTASSIUM NITRATE AND SODIUM FLUORIDE DENTIFRICEXiling (Zhenjiang) Medical Technology Co., Ltd.3f47f399-1a14-5264-e063-6394a90aeb1c2025-09-20WarningsExact identifier
ndc (package): 87118-003-01
ndc (product): 87118-003
ndc11 (package): 87118000301
spl id: 3f47f399-1a15-5264-e063-6394a90aeb1c
spl set id: 3f47f399-1a14-5264-e063-6394a90aeb1c

Reported adverse events (FAERS/openFDA)#

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