Celmark International, Inc.
Celmark International is a dietary supplement contract manufacturer operating a 100,000-square-foot facility at 2600 Titan Row in Orlando, Florida (established 2002), specializing in liquid supplement nutraceuticals including unit-dose liquids, specialty oils, and emulsions. The facility is listed in the NSF public directory as certified to the NSF/ANSI 455-2 dietary supplement Good Manufacturing Practice standard, with liquid formulation and mixing among its listed product technologies. Celmark also produces topical and personal-care formulations. Minimum order quantities and lead times are not publicly posted.
Orlando, Florida
Directory Listing · Certifications Confirmed
One or more certifications independently confirmed via public registries.
What this means →- MOQMOQ (Minimum Order Quantity)The smallest production run a manufacturer will accept for an order.
- Not publicly disclosed
- LEAD TIMELead TimeThe time from order placement to finished product delivery.
- Not publicly disclosed
§1Editorial assessment
Celmark International is a dietary supplement contract manufacturer operating a 100,000-square-foot facility at 2600 Titan Row in Orlando, Florida (established 2002), specializing in liquid supplement nutraceuticals including unit-dose liquids, specialty oils, and emulsions. The facility is listed in the NSF public directory as certified to the NSF/ANSI 455-2 dietary supplement Good Manufacturing Practice standard, with liquid formulation and mixing among its listed product technologies. Celmark also produces topical and personal-care formulations. Minimum order quantities and lead times are not publicly posted.
§2Our review
The six checks in our review, applied before any name appears in the directory. Each check is auto-derived from public evidence on this profile.
§3Inspection history
§4Certifications
1 of 3 certifications independently confirmed. What this means
§5Capability matrix
- PRODUCT TYPES
- Liquids
- CAPABILITIES
- Custom Formulation · Private Label · Liquid Manufacturing · Packaging
- DOSAGE FORMS
- liquids
§6Sources
- Celmark Labs - Official Website(2026-06-24)
- NSF/ANSI 455-2 GMP Directory(2026-06-24)
§7 · What we don't know
- On-site facility inspection was not conducted
- Minimum order quantities and lead times not publicly disclosed
Dietary supplement manufacturers must comply with 21 CFR Part 111 (Current Good Manufacturing Practice for dietary supplements). This includes requirements for personnel, facilities, equipment, production, laboratory operations, and record-keeping.
What We Couldn't Verify
- Minimum order quantities and lead times are not publicly disclosed
- On-site facility inspection was not conducted
- The facility also produces topical and personal-care (cosmetic) products; this assessment covers its dietary-supplement liquid manufacturing scope
Last reviewed: June 24, 2026
Disclosures
- No material connection exists between Inventory Ready and this manufacturer
For the check-by-check breakdown that produces this vendor's score, see our scoring framework. The connection map between Celmark International, Inc. and other vendors, capabilities, and certifications is in the manufacturer atlas.
Our Evaluation Method
Every manufacturer assessment follows six principles:
- Evidence: Claims backed by documentation, not marketing copy
- Freshness: Information reviewed and dated within the last 12 months
- Provenance: Sources cited for every key claim
- Challenge: Inconsistencies flagged, not hidden
- Disclosure: Material connections stated directly on affected listings
- Abstention: When we can't assess, we say so explicitly
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