SENSODYNE PRONAMEL Daily Protection

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: SENSODYNE PRONAMEL Daily Protection
Generic name: POTASSIUM NITRATE AND SODIUM FLUORIDE
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: edffce4d-108b-4ffd-9adf-e12cb42ffddd
SPL ID: 0fb8d5cd-17d5-f0ac-e063-6394a90ab28d
Version: 21
Effective date: 2024-01-24
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 02:01:34

Harmonized routes table
Harmonized routes
ORAL

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 2 · 44 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		SENSODYNE PRONAMEL Fresh Breath	openfda.brand_name
brand name		SENSODYNE PRONAMEL Gentle Whitening	openfda.brand_name
brand name		SENSODYNE PRONAMEL Multi Action	openfda.brand_name
brand name		SENSODYNE PRONAMEL Daily Protection	openfda.brand_name
generic name		POTASSIUM NITRATE AND SODIUM FLUORIDE	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0135-0460-03	openfda.package_ndc
ndc	package	0135-0484-02	openfda.package_ndc
ndc	package	0135-0520-02	openfda.package_ndc
ndc	package	0135-0520-06	openfda.package_ndc
ndc	package	0135-0484-05	openfda.package_ndc
ndc	package	0135-0484-03	openfda.package_ndc
ndc	package	0135-0460-01	openfda.package_ndc
ndc	package	0135-0484-06	openfda.package_ndc
ndc	package	0135-0520-05	openfda.package_ndc
ndc	package	0135-0520-01	openfda.package_ndc
ndc	package	0135-0484-04	openfda.package_ndc
ndc	package	0135-0460-06	openfda.package_ndc
ndc	package	0135-0484-01	openfda.package_ndc
ndc	package	0135-0568-04	openfda.package_ndc
ndc	product	0135-0460	openfda.product_ndc
ndc	product	0135-0568	openfda.product_ndc
ndc	product	0135-0484	openfda.product_ndc
ndc	product	0135-0520	openfda.product_ndc
ndc11	package	00135048403	derived:openfda.package_ndc
ndc11	package	00135048405	derived:openfda.package_ndc
ndc11	package	00135048404	derived:openfda.package_ndc
ndc11	package	00135052001	derived:openfda.package_ndc
ndc11	package	00135056804	derived:openfda.package_ndc
ndc11	package	00135048402	derived:openfda.package_ndc
ndc11	package	00135046001	derived:openfda.package_ndc
ndc11	package	00135052005	derived:openfda.package_ndc
ndc11	package	00135046003	derived:openfda.package_ndc
ndc11	package	00135046006	derived:openfda.package_ndc
ndc11	package	00135052006	derived:openfda.package_ndc
ndc11	package	00135052002	derived:openfda.package_ndc
ndc11	package	00135048401	derived:openfda.package_ndc
ndc11	package	00135048406	derived:openfda.package_ndc
rxcui		1086243	openfda.rxcui

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 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. pain/sensitivity still persists after 4 weeks of use. Keep out of reach of children. 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.