ARC 2 in 1 Whitening and Anticavity

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: ARC 2 in 1 Whitening and Anticavity
Generic name: SODIUM MONOFLUOROPHOSPHATE
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: 12634efa-35e3-76d7-e063-6294a90a3de4
SPL ID: 47e520ba-9f2a-d002-e063-6394a90acac8
Version: 5
Effective date: 2026-01-08
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:18:57

Harmonized routes table
Harmonized routes
ORAL

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		ARC 2 in 1 Whitening and Anticavity	openfda.brand_name
generic name		SODIUM MONOFLUOROPHOSPHATE	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	69423-837-30	openfda.package_ndc
ndc	product	69423-837	openfda.product_ndc
ndc11	package	69423083730	derived:openfda.package_ndc
rxcui		1038995	openfda.rxcui
spl id		47e520ba-9f2a-d002-e063-6394a90acac8	id
spl set id		12634efa-35e3-76d7-e063-6294a90a3de4	set_id
unii		C810JCZ56Q	openfda.unii

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