Sensitive Teeth and Gums

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: Sensitive Teeth and Gums
Generic name: POTASSIUM NITRATE, SODIUM FLUORIDE
Manufacturer: Church & Dwight Co., Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 935172db-d78f-0c69-e053-2a95a90a0b69
SPL ID: 574c1371-6ae8-fd05-e063-6394a90a9e0e
Version: 6
Effective date: 2026-07-23
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:56:32

Harmonized routes table
Harmonized routes
DENTAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M021	openfda.application_number
brand name		Sensitive Teeth and Gums	openfda.brand_name
generic name		POTASSIUM NITRATE, SODIUM FLUORIDE	openfda.generic_name
manufacturer name		Church & Dwight Co., Inc.	openfda.manufacturer_name
ndc	package	10237-669-42	openfda.package_ndc
ndc	package	10237-669-44	openfda.package_ndc
ndc	package	10237-669-45	openfda.package_ndc
ndc	package	10237-669-09	openfda.package_ndc
ndc	product	10237-669	openfda.product_ndc
ndc11	package	10237066944	derived:openfda.package_ndc
ndc11	package	10237066909	derived:openfda.package_ndc
ndc11	package	10237066942	derived:openfda.package_ndc
ndc11	package	10237066945	derived:openfda.package_ndc
rxcui		1038929	openfda.rxcui
spl id		574c1371-6ae8-fd05-e063-6394a90a9e0e	id
spl set id		935172db-d78f-0c69-e053-2a95a90a0b69	set_id
unii		8ZYQ1474W7	openfda.unii
unii		RU45X2JN0Z	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings When using this product do not use longer than 4 weeks 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 by a dentist.

Reported adverse events (FAERS/openFDA)#

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