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AllerBlock-Adult

FDA UDI

Class II (US FDA UDI)

by Wisconsin Pharmacal Co., Llc

Identity

Trade Name
AllerBlock-Adult FDA UDI
Generic Name
Nasal mucosa dressing, non-antimicrobial FDA UDI
Device Name
Powder Nasal Spray FDA UDI
Model / Reference
4210 FDA UDI
Description
Powder Nasal Spray FDA UDI

Identifiers

Primary DI / UDI-DI
00368093000001 FDA UDI
FDA Product Code
NUP FDA UDI
GMDN Term
Nasal mucosa dressing, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5045 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 800 Milligram FDA UDI

Category: Nasal mucosa dressing, non-antimicrobial

AllerBlock-Adult by Wisconsin Pharmacal Co., Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal mucosa dressing, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wisconsin Pharmacal Co., Llc

Sources (1)

  • FDA UDI c0c039f7-c087-4d98-a04d-7202f498536d 36 fields · synced Jun 7, 2026