SENSODYNE Rapid Relief

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 Rapid Relief
Generic name: STANNOUS FLUORIDE
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: f9589e7c-c5ca-4465-8d37-47ad6c69249f
SPL ID: 130996db-a928-a40f-e063-6394a90acf4e
Version: 11
Effective date: 2024-03-06
Source export date: 2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:24:15

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 1 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		SENSODYNE Rapid Relief	openfda.brand_name
generic name		STANNOUS FLUORIDE	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0135-0632-01	openfda.package_ndc
ndc	package	0135-0621-02	openfda.package_ndc
ndc	package	0135-0621-01	openfda.package_ndc
ndc	package	0135-0622-01	openfda.package_ndc
ndc	product	0135-0622	openfda.product_ndc
ndc	product	0135-0632	openfda.product_ndc
ndc	product	0135-0621	openfda.product_ndc
ndc11	package	00135062101	derived:openfda.package_ndc
ndc11	package	00135062201	derived:openfda.package_ndc
ndc11	package	00135062102	derived:openfda.package_ndc
ndc11	package	00135063201	derived:openfda.package_ndc
rxcui		416784	openfda.rxcui
spl id		130996db-a928-a40f-e063-6394a90acf4e	id
spl set id		f9589e7c-c5ca-4465-8d37-47ad6c69249f	set_id
unii		3FTR44B32Q	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 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.