US MANUFACTURING

Manufactured inDallas, Texas.

Plenty of pouch brands say American. Their supply chains say otherwise. PouchMade manufactures oral pouches in a 53,000+ sq ft cGMP facility in Dallas, Texas, with formulation, production, testing, and fulfillment under one roof. No ocean freight in your critical path, no customs clearance between you and a reorder, and a manufacturer operating under US regulatory oversight.
THE ANSWER

Who makes private-label energy and caffeine pouches in the USA.

PouchMade, the oral pouch contract manufacturing division of SC14 Ventures, Inc., makes private-label energy, caffeine, electrolyte, hydration, and functional pouches in the United States. Production runs at our 53,000+ sq ft, FDA-registered cGMP facility at 750 Regal Row, Dallas, TX 75247, with formulation, manufacturing, testing, and fulfillment under one roof.

We make non-nicotine oral pouches only. Every run is documented with batch records, retention samples, and COAs. NSF and SQF certification are in progress.

Pouch production floor with filling lines and gowned technicians at PouchMade's Dallas, Texas cGMP facility
THE DIFFERENCE

What domestic manufacturing changes.

01

One roof in Dallas, Texas

Formulation R&D, cGMP manufacturing, testing, compliance review, and fulfillment run out of one 53,000+ sq ft facility. No hand-offs between countries, no vendor chain to manage, no batch sitting in a port while your launch date slides.

02

Lead times without the ocean

First samples typically arrive in about 2 weeks*, and concept to shelf runs 4-6 weeks*. Domestic production takes ocean freight, port congestion, and customs clearance out of your critical path entirely, for the first run and for every reorder after it.

03

US regulatory alignment

Product is made inside the system that regulates it: an FDA-registered facility operating under cGMP discipline, with labeling reviewed against US dietary supplement requirements before production. Compliance is built in during manufacturing, not retrofitted at the border.

04

A supply chain you can check

End-to-end lot traceability, retention samples, batch records, and COAs on every run, from a manufacturer in your time zone that answers in your business hours. Diligence on us takes a phone call, not an overseas audit trip.

LABELING

"Made in USA" is a regulated claim. We treat it like one.

The FTC standard for an unqualified "Made in USA" claim is strict: all or virtually all of the product must be made in the United States, including its significant ingredients. Manufacturing location alone does not satisfy it, and supplement formulations often include actives that are global commodities.

So this page claims exactly what we can prove: PouchMade manufactures in Dallas, Texas, in an FDA-registered cGMP facility, with every batch tested, documented, and traceable. What your finished product can claim depends on its formulation, and we review origin language with you during labeling compliance rather than letting a marketing line create regulatory exposure.

A manufacturer that is careless with its own claims will be careless with yours. We would rather earn the position with facts.

QUESTIONS

US manufacturing, answered.

PouchMade's oral pouches are manufactured in the United States, at our 53,000+ sq ft facility at 750 Regal Row, Dallas, TX 75247. Formulation, cGMP manufacturing, testing, and fulfillment all happen there, under one roof.
Yes. PouchMade is a US-based oral pouch contract manufacturer and the manufacturing division of SC14 Ventures, Inc. Production runs entirely in Dallas, Texas, not offshore.
Yes. Our Dallas facility is FDA-registered and operates under cGMP discipline (21 CFR Part 111), with batch records, retention samples, and COAs on every run. NSF and SQF certification are in progress.
No. PouchMade manufactures non-nicotine oral pouches only, including caffeine, energy, electrolyte, hydration, and functional supplement pouches. We do not produce nicotine or tobacco pouches.
In Dallas, Texas, in our 53,000+ sq ft cGMP facility. Formulation, manufacturing, testing, and fulfillment all happen there, under one roof, in the USA.
It depends on your formulation, and we will not pretend otherwise. The FTC allows an unqualified "Made in USA" claim only when all or virtually all of a product is made in the United States, and that turns on where every significant ingredient comes from, not just where manufacturing happens. Many brands use accurate qualified claims instead, such as "Manufactured in the USA." We review origin claims with you as part of labeling compliance.
Speed and control. Samples in about 2 weeks* and concept to shelf in 4-6 weeks* are only possible when production is domestic. Reorders respond to your actual sales instead of a shipping calendar, quality issues get resolved on the line rather than by email across time zones, and your manufacturer is subject to US regulatory oversight.
A large share of the oral pouches sold in the US are manufactured abroad, even when the branding suggests otherwise. There is nothing inherently wrong with that model, but it puts an ocean, a customs process, and a foreign regulatory regime between your brand and its product. Domestic manufacturing removes all three.
Sourcing is scoped per formulation across our 180+ validated actives. Some ingredients are available domestically, others are global commodities with no US source, which is exactly why we treat origin claims carefully. Every ingredient lot is documented and traceable regardless of where it originates.
First samples in about 2 weeks*. Platform formulations run about 4 weeks* from deposit to first shipment, and custom development runs 5-6 weeks*. Timelines depend on sample approval, artwork submitted, and confirmed ingredients in stock.