Beaumont Bio-med, Inc. recalls Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed
Beaumont Bio-med recalls Skin Irritation & Itch Response Homeopathic Formula due to possible microbial contamination from manufacturing conditions. Affected products have specific NDC and lot numbers. Consumers should check their bottles for the label details.
Lower-risk recall
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Contact the company & request your remedy
What happened, in plain English
Beaumont Bio-med is recalling their Skin Irritation & Itch Response Homeopathic Formula because it may have been contaminated with microbes during manufacturing. This could lead to skin irritation or other health issues if used. Consumers should stop using the product if they have it. Read more at govinfonow.com/recall/39662-beaumont-bio-med-skin-irritation-itch-response-homeopathic-formula-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/39662-beaumont-bio-med-skin-irritation-itch-response-homeopathic-formula-recall · Updated October 6, 2026 · FDA enforcement record: FDA #D-1192-2018
Cite this page
“Beaumont Bio-med Skin Irritation & Itch Response Homeopathic Formula Recall: Possible Microbial Contamination.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39662-beaumont-bio-med-skin-irritation-itch-response-homeopathic-formula-recall. Based on FDA recall #D-1192-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1192-2018%22&limit=1).
Why it’s dangerous
The product was manufactured under conditions that could result in microbial contamination. This means the formula might contain harmful bacteria or other microorganisms that could cause skin irritation or infections if used.
Who’s affected
People who own or use the Skin Irritation & Itch Response Homeopathic Formula product are affected. Those with sensitive skin or allergies may be at higher risk of irritation.
How to tell if you have this one
Check for the amber glass oral spray bottle labeled 'Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL)'. The product has NDC 58066-7002-7 and specific lot numbers like 091515C (expiring 09/2018) or 050118S (expiring 05/2021).
- Brand
Beaumont Bio-med- Category
Drug
All 8 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Nationwide in the USA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1192-2018 | Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7002-7; Lot: 091515C, Exp 09/2018; 050118S, Exp 05/2021 | 192 bottles |
| D-1193-2018 | Sinus Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7013-7; Lot: 100316A, Exp 10/2019 | 90 bottles |
| D-1194-2018 | Sore Throat & Laryngitis Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7014-7; Lot: 100316G, Exp 10/2019; 050118R, Exp 05/2021 | 420 bottles |
| D-1195-2018 | Diarrhea Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7022-7; Lot: 090915A, Exp 09/2018 | 160 bottles |
| D-1196-2018 | Muscle & Joint Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7041-7; Lot: 012916F, Exp 01/2019 | 109 bottles |
| D-1197-2018 | Allergy & Hay Fever Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7011-7; Lot: 050216X, Exp 05/2019 | 124 bottles |
| D-1198-2018 | Colds & Flu Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7012-7; Lot: 042816C, Exp 04/2019; 112317K, Exp 11/2020 | 314 bottles |
| D-1199-2018 | Arthritis Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7042-7; Lot: 012916E, Exp 01/2019 | 140 bottles |
What to do — step by step
Check Product Label
Look for the NDC number 58066-7002-7 and lot numbers such as 091515C or 050118S on the bottle.
Questions people ask
Is this product safe to use?
The product may have been contaminated with microbes during manufacturing, so it is not recommended for use. Consumers should stop using it if they have it.
What should I do if I have this product?
Check the product label for the NDC number 58066-7002-7 and lot numbers. If you have the affected product, stop using it and contact Beaumont Bio-med for further instructions.
How can I tell if I have the recalled product?
The product is an amber glass oral spray bottle labeled 'Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL)'. It has NDC 58066-7002-7 and lot numbers like 091515C (expiring 09/2018) or 050118S (expiring 05/2021).
Contact Beaumont Bio-med
We’ve drafted a message you can send Beaumont Bio-med to request your refund or repair — edit it as you like.
Subject: Recall D-1192-2018 — Beaumont Bio-med Beaumont Bio-med Hello, I own a Beaumont Bio-med that is covered by recall D-1192-2018 from Beaumont Bio-med. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1192-2018 (August 31, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1192-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.