AQUAFRESH EXTREME CLEAN WHITENING ACTION

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 EXTREME CLEAN WHITENING ACTION
Generic name: SODIUM FLUORIDE
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: aaff19d9-4ba5-462a-893b-7220feb25d6c
SPL ID: 4af3766f-39a7-abd8-e063-6294a90ad4a7
Version: 23
Effective date: 2026-02-16
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:47

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		AQUAFRESH EXTREME CLEAN WHITENING ACTION	openfda.brand_name
generic name		SODIUM FLUORIDE	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0135-0432-02	openfda.package_ndc
ndc	package	0135-0234-08	openfda.package_ndc
ndc	package	0135-0234-06	openfda.package_ndc
ndc	package	0135-0432-05	openfda.package_ndc
ndc	package	0135-0234-09	openfda.package_ndc
ndc	product	0135-0234	openfda.product_ndc
ndc	product	0135-0432	openfda.product_ndc
ndc11	package	00135043202	derived:openfda.package_ndc
ndc11	package	00135023409	derived:openfda.package_ndc
ndc11	package	00135023408	derived:openfda.package_ndc
ndc11	package	00135043205	derived:openfda.package_ndc
ndc11	package	00135023406	derived:openfda.package_ndc
rxcui		1044547	openfda.rxcui
spl id		4af3766f-39a7-abd8-e063-6294a90ad4a7	id
spl set id		aaff19d9-4ba5-462a-893b-7220feb25d6c	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 you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center right away. Keep out of reach of children under 6 years of age. (Whitening Multi Action only) 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.