AQUAFRESH CAVITY 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: AQUAFRESH CAVITY PROTECTION
Generic name: SODIUM FLUORIDE
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: 5484999c-8e6f-430d-99a5-6893a2489467
SPL ID: 4af361ee-0754-8996-e063-6294a90aab2d
Version: 9
Effective date: 2026-02-16
Source export date: 2026-10-30
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/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:01:32

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		AQUAFRESH CAVITY PROTECTION	openfda.brand_name
brand name		AQUAFRESH EXTRA FRESH PLUS WHITENING	openfda.brand_name
generic name		SODIUM FLUORIDE	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0135-0590-01	openfda.package_ndc
ndc	package	0135-0590-05	openfda.package_ndc
ndc	package	0135-0592-01	openfda.package_ndc
ndc	package	0135-0591-01	openfda.package_ndc
ndc	package	0135-0591-02	openfda.package_ndc
ndc	package	0135-0590-02	openfda.package_ndc
ndc	package	0135-0594-01	openfda.package_ndc
ndc	package	0135-0590-04	openfda.package_ndc
ndc	product	0135-0592	openfda.product_ndc
ndc	product	0135-0594	openfda.product_ndc
ndc	product	0135-0591	openfda.product_ndc
ndc	product	0135-0590	openfda.product_ndc
ndc11	package	00135059201	derived:openfda.package_ndc
ndc11	package	00135059101	derived:openfda.package_ndc
ndc11	package	00135059004	derived:openfda.package_ndc
ndc11	package	00135059401	derived:openfda.package_ndc
ndc11	package	00135059102	derived:openfda.package_ndc
ndc11	package	00135059002	derived:openfda.package_ndc
ndc11	package	00135059005	derived:openfda.package_ndc
ndc11	package	00135059001	derived:openfda.package_ndc
rxcui		1044547	openfda.rxcui
spl id		4af361ee-0754-8996-e063-6294a90aab2d	id
spl set id		5484999c-8e6f-430d-99a5-6893a2489467	set_id
unii		8ZYQ1474W7	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, if irritation occurs discontinue use 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.