UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Form 6-K
REPORT OF FOREIGN PRIVATE ISSUER
PURSUANT TO RULE 13a-16 OR 15d-16 UNDER
THE SECURITIES EXCHANGE ACT OF 1934
For the Month of June 2026
Commission File Number: 001-38104
IMMURON LIMITED
(Name of Registrant)
Level 3, 62 Lygon Street, Carlton South,
Victoria, 3053, Australia
(Address of principal executive office)
Indicate by check mark whether the registrant files or will file annual
reports under cover of Form 20-F or Form 40-F.
Form 20-F ☒ Form
40-F ☐
Indicate by check mark whether by furnishing the information contained
in this Form, the registrant is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the Securities
Exchange Act of 1934.
Yes ☐ No
☒
If “Yes” is marked, indicate below the file number assigned
to the registrant in connection with Rule 12g3-2(b): 82-
IMMURON LIMITED
EXPLANATORY NOTE
Immuron Limited (the “Company”) published
an announcement (the “Public Notices”) to the Australian Securities Exchange on June 23, 2026 titled:
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Ummarketable Parcel Facility Update |
A copy of the Public Notice is attached as an exhibit to this report
on Form 6-K.
This report on Form 6-K (including the exhibit
hereto) shall not be deemed to be “filed” for purposes of the Securities Exchange Act of 1934, as amended (the “Exchange
Act”) and shall not be incorporated by reference into any filing under the Securities Act of 1933, as amended, except as shall be
expressly set forth by specific reference in such filing.
EXHIBITS
Exhibit
Number |
|
Description |
| 99.1 |
|
Unmarketable Parcel Facility Update |
SIGNATURE
Pursuant to the requirements of the Securities
Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
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IMMURON LIMITED |
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| Date: June 23, 2026 |
By: |
/s/ Olga Smejkalova |
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|
Olga Smejkalova |
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|
Company Secretary |
Exhibit 99.1

ASX Announcement
23 June 2026
Unmarketable Parcel Facility Update
Immuron Limited (ASX: IMC; NASDAQ: IMRN) (Immuron
or Company) refers to its announcement dated 13 April 2026 and is pleased to announce that it has completed its small holding
share sale facility (Facility).
The Company offered the Facility for shareholders
with less than a marketable parcel based on its share price and share register as at close of trade on 8 April 2026 (Record Date).
Under Australian Securities Exchange (ASX) Listing Rules, a marketable parcel of shares is a parcel of ordinary shares (Shares)
of not less than $500, based on the closing price of the Shares on the ASX.
Under the terms of the Facility, shareholders
who held 18,518 or less Shares in an individual holding at the Record Date were eligible to participate (Eligible Shareholder).
Eligible Shareholders had until 5.00pm (Sydney time) on 1 June 2026 to opt out of the Facility or increase their individual shareholding
to a marketable parcel (Closing Date). Eligible Shareholders that did not exercise either of these options by the Closing Date
have had their Shares acquired (Participating Shareholders).
As previously announced, the Company appointed
Henslow to sell the Shares under the Facility either on the market or in any other manner they consider to be fair and reasonable. Henslow
has advised the Company that the offer from the Company to buy-back the Shares (in accordance with section 257B of the Corporations
Act 2001 (Cth)) at the price of $0.032 per share, being the Volume Weighted Average Price calculated over the 5 trading days (15 June
– 19 June) (Sale Price) is currently the best price reasonably obtainable for the Shares.
Accordingly, the Participating Shareholders will
receive the Sale Price for each Share bought-back by the Company (Buy-back). No brokerage or any other costs were included in calculating
this Sale Price, thereby allowing Participating Shareholders to sell their Shares without incurring any transactional costs.
Any tax consequences arising from the sale of
the Shares will be the Participating Shareholders’ responsibility. Tax may be payable on any gains made on the sale of the Shares.
This will depend on individual personal taxation circumstances. Participating Shareholders should obtain independent tax advice from an
appropriate tax adviser regarding any questions they have about their personal taxation circumstances.


In total, 3,805,528 shares have been acquired
and will be cancelled by the Company, which had an aggregate value of $121,777. The Company expects that following this completion of
the Buy-back, it will reduce the administrative costs of managing small holdings.
As at the Closing Date, the outcome of the Buy-back
on the Company’s capital structure is as follows:
| Number of ordinary shares on issue before completion of the Buy-back | |
| 326,653,609 | |
| Number of shareholders before completion of the Buy-back | |
| 2,264 | |
| Number of ordinary shares on issue after completion of the Buy-back | |
| 322,848,081 | |
| Number of shareholders after completion of the Buy-back | |
| 1,253 | |
The Sale Price will be dispatched to Participating
Shareholders in the coming days to the bank account registered with Boardroom Pty Limited (Share Registry). If Participating Shareholders
bank account details are not up to date or not recorded, a cheque will be sent to the postal address as shown in the share register.
This announcement has been authorised by the
Board of Immuron.
- - - END - - -
COMPANY CONTACT:
Steven Lydeamore
Chief Executive Officer
steve@immuron.com
About Immuron
Immuron
Limited (ASX: IMC, NASDAQ: IMRN), is an Australian biopharmaceutical company focused on developing and commercializing orally delivered
targeted polyclonal antibodies for the treatment of infectious diseases.
About Travelan®
Travelan® is an
orally administered passive immunotherapy that prophylactically reduces the likelihood of contracting travelers’ diarrhea, a
digestive tract disorder that is commonly caused by pathogenic bacteria and the toxins they produce. Travelan® is a highly
purified tabletized preparation of hyper immune bovine antibodies and other factors, which when taken with meals bind to diarrhea-causing
bacteria and prevent colonization and the pathology associated with travelers’ diarrhea. In Australia, Travelan® is a listed
medicine on the Australian Register for Therapeutic Goods (AUST L 106709) and is indicated to reduce the risk of Travelers’ Diarrhea,
reduce the risk of minor gastro-intestinal disorders and is antimicrobial. In Canada, Travelan® is a licensed natural health product
(NPN 80046016) and is indicated to reduce the risk of Travelers’ Diarrhea. In the U.S., Travelan® is sold as a dietary supplement
for digestive tract protection.


Immuron Platform Technology
Immuron’s proprietary
technology is based on polyclonal immunoglobulins (IgG) derived from engineered hyper-immune bovine colostrum. Immuron has the capability
of producing highly specific immunoglobulins to any enteric pathogen and our products are orally active. Bovine IgG can withstand the
acidic environment of the stomach and is resistant to proteolysis by the digestive enzymes found in the Gastrointestinal (GI) tract. Bovine
IgG also possesses this unique ability to remain active in the human GI tract delivering its full benefits directly to the bacteria found
there. The underlying nature of Immuron’s platform technology enables the development of medicines across a large range of infectious
diseases. The platform can be used to block viruses or bacteria at mucosal surfaces such as the Gastrointestinal tract and neutralize
the toxins they produce.
For more information
visit: https://www.immuron.com.au/ and https://www.travelan.com
Subscribe to Immuron’s
InvestorHub: Here
FORWARD-LOOKING STATEMENTS:
This press release may contain “forward-looking
statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934,
each as amended. Such statements include, but are not limited to, any statements relating to our growth strategy and product development
programs and any other statements that are not historical facts. Forward-looking statements are based on management’s current expectations
and are subject to risks and uncertainties that could negatively affect our business, operating results, financial condition, and stock
value. Factors that could cause actual results to differ materially from those currently anticipated include: risks relating to our growth
strategy; our ability to obtain, perform under and maintain financing and strategic agreements and relationships; risks relating to the
results of research and development activities; risks relating to the timing of starting and completing clinical trials; uncertainties
relating to preclinical and clinical testing; our dependence on third-party suppliers; our ability to attract, integrate and retain key
personnel; the early stage of products under development; our need for substantial additional funds; government regulation; patent and
intellectual property matters; competition; as well as other risks described in our SEC filings. We expressly disclaim any obligation
or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in
our expectations or any changes in events, conditions, or circumstances on which any such statement is based, except as required by law.
