Seavue Dental Desensitizer

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Seavue Dental Desensitizer
Generic name
POTASSIUM NITRATE AND SODIUM FLUORIDE DENTIFRICE
Manufacturer
Xiling (Zhenjiang) Medical Technology Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
3f47f399-1a14-5264-e063-6394a90aeb1c
SPL ID
3f47f399-1a15-5264-e063-6394a90aeb1c
Version
1
Effective date
2025-09-20
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:59:45
Harmonized routes table
Harmonized routes
DENTAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

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