SupraNaturals
Contract manufacturer of liquids, powders, chewables, softgels and stick packs, with in-house R&D.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
SupraNaturals is a contract manufacturer operating a facility of more than 300,000 square feet in Springville, Utah, serving the nutraceutical, dietary supplement, and functional food markets. The company manufactures a broad mix of form factors including liquids, powders, capsules, tablets, chewables, softgels, and stick packs, alongside personal care, CBD and hemp formats. Services include product development, custom formulation, in-house research and development, and full-scale production. The company is listed in the NPA GMP Certified Companies public directory (listing checked 2026-06-11). The company markets itself as a single-site supplier capable of handling both emerging and established brand volumes.
Certifications
0 of 1 certification independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Liquids · Powders · Capsules · Tablets · Chewables · Softgels · Stick Packs
- CAPABILITIES
- Custom formulas · R&D or product development · Packaging · Personal care products
- DOSAGE FORMS
- liquids · powders · capsules · tablets · chewables · softgels · stick-packs
Sources
- SupraNaturals Official Website(2026-05-25)
- NPA GMP Certified Companies Directory(2026-05-25)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- Founded date not disclosed publicly
- Additional facility-level certifications beyond NPA GMP not enumerated
- Detail on CBD and hemp regulatory positioning not surfaced
- Founded date not surfaced from public materials
- Additional facility certifications (NSF, UL, SQF) not enumerated on the public website at this assessment
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between SupraNaturals 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 →
Our Evaluation Method
A full assessment applies six checks. Source-Checked listings get a lighter review.
- Independent confirmation: Claims backed by documentation, not marketing copy
- How recent the data is: Information reviewed and dated within the last 12 months
- Sources we traced: Sources cited for every key claim
- Inconsistencies flagged: Where a company's claims and public records disagree, we say so
- What we disclose: Material connections stated directly on affected listings
- What we don't know: When we can't assess something, we say so explicitly
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