PerioRestore

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: PerioRestore
Generic name: HYDROGEN PEROXIDE
Manufacturer: DEN-MAT HOLDINGS, LLC.
Product type: HUMAN OTC DRUG
SPL set ID: 97a07c36-1af8-a636-e053-2a95a90ad6db
SPL ID: 0a0d08d7-e3f3-d98d-e063-6394a90af5e9
Version: 3
Effective date: 2023-11-13
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:32:16

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		PerioRestore	openfda.brand_name
generic name		HYDROGEN PEROXIDE	openfda.generic_name
manufacturer name		DEN-MAT HOLDINGS, LLC.	openfda.manufacturer_name
ndc	package	59883-018-87	openfda.package_ndc
ndc	product	59883-018	openfda.product_ndc
ndc11	package	59883001887	derived:openfda.package_ndc
rxcui		1095271	openfda.rxcui
spl id		0a0d08d7-e3f3-d98d-e063-6394a90af5e9	id
spl set id		97a07c36-1af8-a636-e053-2a95a90ad6db	set_id
unii		BBX060AN9V	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 Do not use Perio Restore Gel for more than 7 days unless directed by your dentist or physician. Stop use and ask your dentist or physician if: Symptoms of wounds or inflammation do not improve within 7 days. Irritation, pain or redness persists or worsens Swelling, rash or fever develops

Reported adverse events (FAERS/openFDA)#

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