Perox-A-Mint Solution

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: Perox-A-Mint Solution
Generic name: HYDROGEN PEROXIDE
Manufacturer: Sage Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 50823ff5-ad08-4449-bc4a-9a8ae25ec0d5
SPL ID: 550655a0-abc2-dae6-e063-6294a90a995f
Version: 15
Effective date: 2026-06-24
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:36:42

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		Perox-A-Mint Solution	openfda.brand_name
generic name		HYDROGEN PEROXIDE	openfda.generic_name
manufacturer name		Sage Products, LLC	openfda.manufacturer_name
ndc	package	53462-075-60	openfda.package_ndc
ndc	package	53462-075-30	openfda.package_ndc
ndc	package	53462-075-40	openfda.package_ndc
ndc	product	53462-075	openfda.product_ndc
ndc11	package	53462007540	derived:openfda.package_ndc
ndc11	package	53462007560	derived:openfda.package_ndc
ndc11	package	53462007530	derived:openfda.package_ndc
rxcui		358975	openfda.rxcui
rxcui		1866540	openfda.rxcui
spl id		550655a0-abc2-dae6-e063-6294a90a995f	id
spl set id		50823ff5-ad08-4449-bc4a-9a8ae25ec0d5	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: For more than 7 days unless told to do so by a doctor. Avoid swallowing. Stop use and ask a doctor if: Sore mouth symptoms do not improve in 7 days. Swelling, rash or fever develops. Irritation, pain or redness persists of worsens. Keep out of reach of children. If more than used for debriding 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.