Peroxyl Mouth Sore Mild Mint

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: Peroxyl Mouth Sore Mild Mint
Generic name: HYDROGEN PEROXIDE
Manufacturer: Colgate Oral Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b1e1b7c9-dea7-4d64-b6a8-5343f4176359
SPL ID: 0df671b6-d668-41ee-935d-838a62924b58
Version: 18
Effective date: 2024-11-25
Source export date: 2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:40:41

Harmonized routes table
Harmonized routes
BUCCAL

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		Peroxyl Mouth Sore Mild Mint	openfda.brand_name
generic name		HYDROGEN PEROXIDE	openfda.generic_name
manufacturer name		Colgate Oral Pharmaceuticals Inc.	openfda.manufacturer_name
ndc	package	0126-0083-22	openfda.package_ndc
ndc	package	0126-0083-31	openfda.package_ndc
ndc	package	0126-0083-99	openfda.package_ndc
ndc	package	0126-0083-16	openfda.package_ndc
ndc	package	0126-0083-70	openfda.package_ndc
ndc	product	0126-0083	openfda.product_ndc
ndc11	package	00126008331	derived:openfda.package_ndc
ndc11	package	00126008399	derived:openfda.package_ndc
ndc11	package	00126008322	derived:openfda.package_ndc
ndc11	package	00126008316	derived:openfda.package_ndc
ndc11	package	00126008370	derived:openfda.package_ndc
rxcui		358975	openfda.rxcui
rxcui		1727009	openfda.rxcui
spl id		0df671b6-d668-41ee-935d-838a62924b58	id
spl set id		b1e1b7c9-dea7-4d64-b6a8-5343f4176359	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 this product for more than 7 days unless directed by a dentist or physician. When using this product, do not swallow. Stop use and ask a doctor if sore mouth symptoms do not improve within 7 days irritation, pain or redness persists or worsens swelling, rash or fever develops Keep out of reach of children. If more than used for rinsing 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.