Auraglow 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: Auraglow Whitening
Generic name: SODIUM FLUORIDE
Manufacturer: Auraglow LLC
Product type: HUMAN OTC DRUG
SPL set ID: 9d45e436-92f6-4a9e-9b82-329847dca9ba
SPL ID: 3f72b20e-32ad-468c-a67b-ff438c3a8396
Version: 1
Effective date: 2025-10-22
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:38:15

Harmonized routes table
Harmonized routes
DENTAL

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M021	openfda.application_number
brand name		Auraglow Whitening	openfda.brand_name
generic name		SODIUM FLUORIDE	openfda.generic_name
manufacturer name		Auraglow LLC	openfda.manufacturer_name
ndc	package	81740-003-03	openfda.package_ndc
ndc	product	81740-003	openfda.product_ndc
ndc11	package	81740000303	derived:openfda.package_ndc
rxcui		1489127	openfda.rxcui
spl id		3f72b20e-32ad-468c-a67b-ff438c3a8396	id
spl set id		9d45e436-92f6-4a9e-9b82-329847dca9ba	set_id
unii		8ZYQ1474W7	openfda.unii

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

Warnings

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