Antiseptic Mouth Sore

Product NDC
69842-515
11-digit product format
698420515
Labeler code
69842
Product ID
69842-515_0a849f0b-2906-4859-bf06-b7562f54310d
Type
HUMAN OTC DRUG
Nonproprietary name
hydrogen peroxide, menthol
Dosage form
RINSE
Route
PERIODONTAL
Labeler
CVS Pharmacy
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-06-18
Marketing end
0000-00-00
Substance
HYDROGEN PEROXIDE; MENTHOL, UNSPECIFIED FORM
Active strength
15 mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct69842-515DDiscontinued by firm2026-10-05
excluded packagepackage69842-51569842-515-43DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage69842-515-43d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage69842-515-43f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-515-4369842051543473 mL in 1 BOTTLE (69842-515-43) 473 ml2021-06-180000-00-00NoNoCurrent