Paragon Laboratories
Maker of tablets, capsules and powders with in-house analytical and microbiological laboratories.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Paragon Laboratories is a contract manufacturer of dietary supplements operating from 20433 Earl Street in Torrance, California. Founded in 1971, the company specializes in custom formulation, manufacturing, and packaging of tablets, capsules, and powders in a range of sizes and configurations. The facility includes production, packaging, and warehousing functions alongside in-house analytical and microbiological laboratories. The company is listed in the NPA GMP Certified Companies public directory (listing checked 2026-06-11); its NSF/ANSI 455-2 GMP certification was registry-confirmed the same day (NSF lists the company as Naturalife Eco Vite Labs., Inc. DBA Paragon Laboratories), and it self-reports UL cGMP audits as part of a triple-GMP positioning. Services span private label, contract manufacturing, custom formulation, and finished-product packaging. The company describes itself as a full-service supplier serving both established and emerging nutraceutical brands.
Certifications
1 of 3 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Tablets · Capsules · Powders
- CAPABILITIES
- Custom formulas · Private label or white label · Packaging
- DOSAGE FORMS
- tablets · capsules · powders
Sources
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- UL cGMP listing not located via UL public directory in this assessment
- UL cGMP claim is self-reported and not independently verified against third-party directories; NSF/ANSI 455-2 was registry-confirmed 2026-06-11 (NSF lists the DBA parent Naturalife Eco Vite Labs)
- Minimum order quantities not surfaced from public materials
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Paragon Laboratories and other vendors, capabilities, and certifications is in the manufacturer atlas.
Enforcement screening: included in Inventory Ready's most recent completed pass against FDA's published recall datasets (2026-07-09). Method and limits →
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