Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2248903

FEI Number

3000206585

Entity Name

BAYER HEALTHCARE LLC, CONSUMER CARE

City/State/Country

MORRISTOWN, NJ, US

Establishment Address

36 Columbia Rd, MORRISTOWN, NJ 07960, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

BAYER HEALTHCARE LLC, CONSUMER CARE DIVISION (Owner Number: 9047714)

Owner / Operator Contact Address

100 Bayer Boulevard, PO Box 915, Whippany, NJ 07981, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Afrin Saline Burst Extra Strength Daily Nasal Mist Children's Afrin Saline Moisturizing Daily Nasal Mist Afrin Saline Daily Care Nasal Mist Afrin Saline Burst Moisturizing Daily Nasal Mist

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCO	Nasal Spray, Ent Delivery	Ear, Nose, Throat	Class 1	874.5220	2024-11-21

Official Correspondent

Sravani Ravi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BAYER HEALTHCARE LLC, CONSUMER CARE DIVISION

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2248903. Last updated year: 2026. Please use registration number 2248903 when referencing this establishment in official correspondence.