Vitalpax
Maker of capsules, tablets, softgels, stick packs, liquids and concentrates, with in-house R&D.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Vitalpax operates an FDA-registered, cGMP-compliant facility in La Verkin, Utah. Founded in 2014, they are listed as certified organic in the USDA Organic Integrity Database and report NSF, Halal, and Kosher certifications. Their facility produces capsules, tablets, softgels, powders, stick packs, liquids, and concentrates. They offer in-house R&D with access to over 7,000 ingredients, third-party testing (HPLC, FTIR), and Amazon registration support. They serve brands of varying sizes with both large and small batch capabilities. The company is a member of NPA and NASC, and is BBB accredited.
Certifications
1 of 6 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Capsules · Tablets · Softgels · Powders · Stick Packs · Liquids · Concentrates
- CAPABILITIES
- Custom formulas · Private label or white label · Packaging · Quality control or lab testing · Regulatory or compliance help
- DOSAGE FORMS
- capsules · liquids · powders · softgels · tablets
Sources
- Vitalpax - Official Website(2026-03-26)
- Vitalpax - Certifications Page(2026-03-26)
- USDA Organic Integrity Database(2026-03-28)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- Email address not publicly listed on website
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Vitalpax 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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