Trusted Partner

Frequently Asked Questions

 Answers to the questions we hear most from brands, retailers, and product developers.

If you do not find what you are looking for here, reach out to our team directly.

We are happy to answer any questions about our capabilities, certifications, or process.

ABOUT PHARMALOZ


What does Pharmaloz manufacture?

Pharmaloz manufactures lozenges exclusively. We produce hard candy lozenges, liquid-filled lozenges, medicated OTC lozenges, dietary supplement lozenges, organic and natural lozenges, and specialty formats including sugar-free, Kosher, and allergen-free products.

Pharmaloz is located at 500 N 15th Ave, Lebanon, Pennsylvania 17046. Our central Pennsylvania location provides direct access to I-78, I-81, and I-83, enabling efficient nationwide distribution.

Pharmaloz has been manufacturing lozenges since 1985, giving us over 35 years of dedicated experience in the lozenge category. Our roots in confectionery manufacturing go back even further, to 1949.

Pharmaloz was acquired by a private family ownership group in January 2025. The new ownership has invested $10 million in facility upgrades including new cooking infrastructure and robotic packaging automation.

Yes. Pharmaloz is a Contract Development and Manufacturing Organization, or CDMO. We offer end-to-end services including custom formulation, contract manufacturing, private label programs, packaging, warehousing, and distribution, all under one roof.

CERTIFICATIONS AND COMPLIANCE


What certifications does Pharmaloz hold?

Pharmaloz holds the following certifications: FDA Registered Facility under 21 CFR Parts 210 and 211, QAI-Organic Certificationc, GMP Certified, USDA Organic Certified, Kosher Certified, UL Certified, Non-GMO, and Made in the USA.

FDA 21 CFR Parts 210 and 211 are the federal regulations governing Current Good Manufacturing Practice for pharmaceutical products, including OTC drug products. Manufacturing under these standards means our facility, processes, documentation, and quality controls meet the same regulatory requirements applied to prescription drug manufacturing.

Yes. Pharmaloz is USDA Organic certified, which means we can manufacture certified organic lozenges that carry the USDA Organic seal. This certification is rare among lozenge contract manufacturers and covers ingredient sourcing, facility standards, and documentation requirements.

Yes. Pharmaloz holds Kosher certification across our manufacturing operations. Kosher certified lozenges are available across medicated, supplement, organic, and specialty product lines.

Yes. Non-GMO formulations are available across our product lines. We source Non-GMO ingredients and maintain the documentation required to support Non-GMO product claims.

FORMULATION AND R&D


Can Pharmaloz develop a custom lozenge formula from scratch?

Yes. Our on-site R&D team develops custom lozenge formulas based on your active ingredients, flavor profile, delivery requirements, and target market. We work with you from initial concept through final formula approval.

Development timelines vary depending on the complexity of the formula, the active ingredients involved, and the number of sample iterations required. In general, expect a formulation development process of several weeks to a few months before moving into production. Our team will give you a specific timeline estimate based on your product.

Yes. If you have an existing formula, our team can review it, assess its manufacturability on our lines, and move it into production. We can also recommend optimizations if needed.

We work with a wide range of active ingredients including menthol, benzocaine, zinc, vitamin C, elderberry, melatonin, probiotics, vitamin B12, and enzymes, among others. If you have a novel or proprietary activity, reach out and we will assess compatibility with our formulation and manufacturing capabilities.

Yes. Liquid-filled and flavor-burst lozenges are a core capability at Pharmaloz. We manufacture both medicated and non-medicated liquid-filled formats, and our 2025 facility investment included upgrades specifically designed to expand our liquid-fill capacity.

PRIVATE LABEL


What is Pharmaloz's private label program?

Our private label program gives retailers, brokers, and brands access to a portfolio of tested, retail-ready lozenge formulas that can be branded and brought to market without a full custom development cycle. We handle manufacturing, packaging, compliance labeling, and distribution.

Our private label portfolio covers cough and throat, immune support, dietary supplements, liquid-filled formats, organic and natural, and specialty formats including sugar-free, Kosher, and allergen-free lozenges.

Yes. USDA Organic and Non-GMO certified options are available within our private label program for brands targeting clean-label and natural product markets.

PRODUCTION AND TIMELINES


What is the minimum order quantity for lozenge manufacturing?

Minimum order quantities vary depending on the product type, format, and packaging requirements. Contact our team or submit a quote request and we will provide specifics based on your product.

Production lead times depend on order volume, packaging complexity, and current production schedules. Our team will provide a specific lead time estimate as part of your quote.

Yes. We source and quality-verify raw materials before production begins. All ingredients are reviewed against your product specifications and our internal quality standards before they enter the production process.

Yes. We offer on-site warehousing for both raw materials and finished goods, along with nationwide distribution from our Lebanon, Pennsylvania facility. Our location provides direct access to major interstate corridors for efficient shipping across the continental United States.

PACKAGING


What packaging formats does Pharmaloz offer?

We offer twist wrap, flow wrap, retail carton packing, and case packing. Custom artwork and compliance labeling support is included as part of our packaging service.

Yes. Our team reviews label copy for regulatory alignment as part of the packaging process. For OTC drug products, this includes compliance with applicable FDA labeling requirements.