Question 1

What dosage forms do you manufacture?

Accepted Answer

Liquids — including tinctures, oil-based products, and liposomes — in 1 oz through 64 oz formats with glass, PET, or HDPE packaging. Capsules are powder-only in sizes #1, #0, #00, and #00E, bottled from 15 ct through 180 ct. Downstream encapsulation, packaging & bottling, and labeling stay inside our published capabilities.

Question 2

Which certifications govern production?

Accepted Answer

Facilities operate under NSF cGMP and NSF Certified for Sport® with production aligned to 21 CFR Part 111 and GDP standards wherever we control the activity.

Question 3

What are your published MOQs?

Accepted Answer

Toll projects publish a 5,000-unit MOQ. Selective custom work lists a 10,000-unit MOQ, with ideal purchase orders in the 10,000–30,000 unit band. White label / catalog lines begin at 250 units with price breaks up to 10,000 units.

Question 4

How do lead times work?

Accepted Answer

Timelines depend on documentation completeness, raw material arrival, and slot availability. We communicate realistic buffers up front — rush promises without qualified schedules are not part of our model.

Question 5

What documentation do brands receive?

Accepted Answer

Expect batch records, COAs, specifications, and release documentation consistent with NSF cGMP and NSF Certified for Sport® operations in a Part 111-aligned system. Exact packets vary by project type but always prioritize traceability.

Question 6

Do you take every formulation project?

Accepted Answer

No. Formulations are reviewed case by case. We decline projects that require services we do not offer — for example stand-alone flavor formulation — or categories that violate our compliance guardrails, such as spore-forming probiotics or high-regulatory-risk ingredients like Delta-8, Kratom, or DMSA.

Question 7

Who is the ideal partner?

Accepted Answer

Proven brands shipping roughly 40,000–300,000 units annually (around $800K–$15M in revenue) with manageable SKUs and appetite for repeat runs. Operators who bring organized documentation, realistic timelines, and respect for GMP systems succeed here.

Supplement Manufacturing FAQ