Opalescence Sensitivity Relief Whitening

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: Opalescence Sensitivity Relief Whitening
Generic name: POTASSIUM NITRATE AND SODIUM FLUORIDE
Manufacturer: Ultradent Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b5176a84-76a3-4ad0-a2e2-4997a12da9a5
SPL ID: 5b14ddfe-ec8e-3a25-e063-6294a90afe5b
Version: 12
Effective date: 2026-09-09
Source export date: 2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:29

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 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		Opalescence Sensitivity Relief Whitening	openfda.brand_name
generic name		POTASSIUM NITRATE AND SODIUM FLUORIDE	openfda.generic_name
manufacturer name		Ultradent Products, Inc.	openfda.manufacturer_name
ndc	package	51206-308-03	openfda.package_ndc
ndc	package	51206-308-05	openfda.package_ndc
ndc	package	51206-308-06	openfda.package_ndc
ndc	package	51206-308-02	openfda.package_ndc
ndc	package	51206-308-01	openfda.package_ndc
ndc	package	51206-308-04	openfda.package_ndc
ndc	product	51206-308	openfda.product_ndc
ndc11	package	51206030806	derived:openfda.package_ndc
ndc11	package	51206030801	derived:openfda.package_ndc
ndc11	package	51206030803	derived:openfda.package_ndc
ndc11	package	51206030804	derived:openfda.package_ndc
ndc11	package	51206030802	derived:openfda.package_ndc
ndc11	package	51206030805	derived:openfda.package_ndc
rxcui		1086243	openfda.rxcui
spl id		5b14ddfe-ec8e-3a25-e063-6294a90afe5b	id
spl set id		b5176a84-76a3-4ad0-a2e2-4997a12da9a5	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 Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. See your dentist if the problem persists or worsens. Do not use this product longer than 4 weeks unless recommended by a dentist or doctor. Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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