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Canker-X Rincinol Mouth Sore Rinse

FDA UDI

Class U (US FDA UDI)

by Alliance Pharma Inc.

Identity

Trade Name
Canker-X Rincinol Mouth Sore Rinse FDA UDI
Generic Name
General oral wound dressing, non-animal-derived FDA UDI
Device Name
Canker-X Rincinol Mouth Sore Rinse 120ml FDA UDI
Model / Reference
Lot Code FDA UDI
Description
Canker-X Rincinol Mouth Sore Rinse 120ml FDA UDI

Identifiers

Primary DI / UDI-DI
00358962302008 FDA UDI
510(k) Number
K023155 FDA UDI
FDA Product Code
MGQ FDA UDI
GMDN Term
General oral wound dressing, non-animal-derived FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General oral wound dressing, non-animal-derived

Canker-X Rincinol Mouth Sore Rinse by Alliance Pharma Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General oral wound dressing, non-animal-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alliance Pharma Inc.

Sources (1)

  • FDA UDI 5fbc05d9-eade-49a6-b8a8-c8fa8f477496 34 fields · synced May 30, 2026