Question 1

Do you support both custom formulations and private label stock products?

Accepted Answer

Yes. Our R&D team develops fully custom formulations from your ingredient deck or concept, and we also offer ready-to-brand private label stock formulas that shorten development time to labeling and packaging only.

Question 2

What are your minimum order quantities (MOQs)?

Accepted Answer

Private label stock formulas typically start at 5,000 units. Custom formulations are quoted by dosage form, active ingredient cost and packaging format, with volume pricing tiers available at 10,000, 50,000 and 100,000+ units.

Question 3

What are your standard manufacturing lead times?

Accepted Answer

Quotes are typically returned within 48 hours, R&D pilot samples within about 5 working days, and standard turnkey production runs approximately 8 weeks from final approval, depending on raw material availability and packaging lead times.

Question 4

What certifications does your facility hold?

Accepted Answer

Our 70,000 sq. ft. Fort Myers, Florida facility is NSF GMP registered, cGMP compliant and FDA registered, with Made in USA production plus USDA Organic ingredient support, Halal ingredient sourcing and Kosher production options.

Question 5

What quality control and product testing do you perform?

Accepted Answer

Every batch follows documented cGMP procedures: raw material identity verification, in-process checks, finished product testing for potency, microbial limits and heavy metals, plus retained samples, batch records and Certificates of Analysis.

Question 6

Can you help with Amazon and international compliance documentation?

Accepted Answer

Yes. We supply Certificates of Analysis, GMP certificates, ingredient specifications, allergen and nutritional data, and supporting documents commonly requested by Amazon Seller Central and international importers.