Contract supplement manufacturing for established brands
F.A.M.E. Health Labs is a high-volume contract supplement manufacturer in Cedartown, Georgia. Our campus encapsulates 100M+ capsules a day and fills 100K+ bottles a day, with formulation, manufacturing and ISO/IEC 17025 testing on one 152-acre campus. Enterprise enquiries get a reply within 4 hours during business hours.
Plus 400M+ stick packs a year on purpose-built lines. Planned: capacity doubling by Q4 2026.
Lead times built for repeat volume.
Four weeks is the production clock on repeat and stock runs of 30,000+ units, against a 12 to 16 week industry norm. The lead time starts when the sales order is signed and the deposit is paid.
Repeat and stock runs of 30,000+ units
Four weeks from production start.
Stock runs under 30,000 units
6 to 8 weeks after formula approval.
Custom formulas
8 to 12 weeks in total.
Gummies and softgels
Plan on about 18 to 20 weeks from quote to a finished first order, depending on the formulation.
What an enterprise program includes.
Enterprise partners work with one team across every product, with the same campus, lab and data behind each run.
A dedicated account manager
One person who owns your program from the first run onward.
Multi-SKU program management
One schedule across every product, format and pack size in your range.
A real-time client portal
Live production status, incoming QC, your certificate of analysis library and spend analytics across every SKU.
A reply within 4 hours
Enterprise enquiries get an answer within 4 hours during business hours.
Testing on campus
Every batch gets identity and microbial testing in curí, our ISO/IEC 17025-accredited lab, and ships with a certificate of analysis. Potency, heavy metals, pesticides and stability testing are available.
Ingredients on site
More than 10,000 raw actives are held on campus, with cycle counts within 24 hours, so formulation starts from stock.
Moving an existing product to F.A.M.E.
Already selling the product? Send us what you have. A technical review confirms specifications, raw-material sourcing, packaging and testing, and flags any difference that needs your approval. A validation run is always done for powders and liquids; for capsules it depends on the product.
The formula
The current formula or Supplement Facts.
Dosage form and count
The format and the count per pack.
Packaging
Bottle, pouch, sachet or stick pack, with closures and labels.
Volume
Your order quantity or annual volume.
Testing and certifications
Any testing or certifications your buyers require.
A current sample
Ideally, a sample of the product as it sells today.
Every major format, one campus.
Capsules, tablets, powders, gummies and liquids are manufactured on our campus, along with sachets and stick packs. Bottling and labeling are in-house.
Certified for retail and enterprise audits.
An FDA-registered facility, certified to cGMP (21 CFR Part 111), SQF (Edition 9) and NSF/ANSI 455-2, with MOSA Certified Organic and a Health Canada Site Licence. Every batch is tested in curí, our ISO/IEC 17025:2017-accredited lab on campus. Halal and Kosher certification is issued per product. Facility visits are by appointment, and certificates are available on request.
Start an enterprise inquiry.
Tell us about the program. An enterprise specialist replies within 4 hours during business hours.
Enterprise manufacturing questions.
Straight answers for procurement and supply teams.
How much can F.A.M.E. manufacture a day?
100M+ capsules, 100K+ bottles, 50K+ sachets and stick packs, and 40K+ powder bottles a day, plus 400M+ stick packs a year on purpose-built lines. Capacity is planned to double by Q4 2026.
How fast are repeat orders?
Repeat and stock runs of 30,000+ units take four weeks from production start. Stock runs under 30,000 units take 6 to 8 weeks after formula approval, and custom formulas 8 to 12 weeks in total.
Can you take over a product we already sell?
Yes. Send the current formula or Supplement Facts, dosage form and count, packaging, annual volume, required testing or certifications, and ideally a sample. A technical review confirms specifications, sourcing, packaging and testing before the first run.
Which certifications does the facility hold?
FDA-registered, cGMP (21 CFR Part 111), SQF (Edition 9), NSF/ANSI 455-2, MOSA Certified Organic and a Health Canada Site Licence. Our on-campus lab, curí, is ISO/IEC 17025:2017 accredited. Halal and Kosher certification is issued per product.
How quickly do you respond to enterprise enquiries?
Within 4 hours during business hours.
