Your Brand.
Our Pouches.
White label & private label nicotine pouches and nicotine-free pouches (caffeine, wellness, herbal) — pharma-grade ingredients, in-house lab tested, manufactured exclusively for the US market since 2018.
PMTA-Aware Manufacturing
Full documentation provided to support your US FDA Premarket Tobacco Application filing.
Two paths to
your brand
Nicotine pouches and caffeine pouches — same pharma-grade facility, same in-house lab, same on-time delivery to your US warehouse.
White Label
Take our proven, pharma-grade formulations and launch under your brand. Available in nicotine (3mg–22mg) and caffeine (50mg, 100mg) pouches.
- Ready pharma-grade formulas — no R&D wait
- Your logo, can design & packaging
- In-house lab CoA every batch
- 4–6 weeks production + shipping to US
- MOQ 50,000 cans (min 5,000 per SKU)
- US compliance labeling included
Private Label
Your exclusive formula, developed by our R&D team and owned entirely by your brand. No competitor can ever replicate it.
- Proprietary flavor — exclusive to your brand forever
- Custom nicotine strength (any mg) or caffeine dose
- Custom pouch format & moisture level
- Full packaging & brand design support
- 8–12 weeks from approval to US delivery
- Complete PMTA documentation support (nicotine)
Your Brand. Our Manufacturing.
100% white label and private label. Pharma-grade manufacturing built around your brand — not ours.
Holographic premium can design. Pharma-grade USP nicotine. Full FDA-compliant labeling. Shipped from our pharma-grade manufacturing facility direct to US distributors since 2018.
Energy alternative to coffee & energy drinks. Five launch flavors. No PMTA required, no age restriction. Growing market — your white label opportunity.
Your formula. Your brand. Manufactured in our pharma-grade facility — exclusively for you. 100% white label and private label. Every can we produce carries your brand only.
The difference matters
Indian FDA Approved
Full CDSCO pharmaceutical regulatory approval. We operate as a pharma facility — not a food factory.
Pharma-Grade Standards
Pharmaceutical-standard production processes, equipment, and documentation. Every batch fully traceable.
Pharma-Grade Ingredients
Every ingredient — nicotine, base, sweeteners, flavors — meets pharmaceutical specification. Not food-grade. Pharma-grade.
In-House Lab Testing
Our own laboratory tests every batch for nicotine accuracy, purity, and safety before it leaves our facility.
USA Market Only
Every flavor, formulation, and compliance document is built exclusively for the United States.
On-Time Delivery
Your US launch timeline is confirmed in writing before production starts. We deliver — every time.
Pharma-grade pouches.
Manufactured to scale.
Our manufacturing facility operates under pharmaceutical-grade quality standards with CDSCO regulatory approval. Shipping pouches to the US market since 2018 — with a proven track record across both nicotine and nicotine-free categories.
Production teams in full sterile PPE. Precision Korean & Japanese filling lines (Hanyoo, CVC). In-house lab testing on every batch. The same pharma-grade facility, the same precision, the same quality control — every can produced exclusively for your white label or private label order.
On-time delivery.
Every time.
Your launch date is a real commitment. We build production around your US timeline — not the other way around.
Timeline Confirmed in Writing
Delivery schedule agreed before production starts. No surprises.
In-House Lab Verified Pre-Dispatch
Every batch tested in our own lab. CoA ships with every order.
Direct to Your US Location
Shipped to your US warehouse, 3PL, or fulfillment center with full tracking.
Full Export Documentation
All Indian export paperwork, customs certificates, and compliance records prepared and included.
19 US-ready flavors.
Or bring your own.
All white label ready. All can be starting point for private label. Custom flavors developed exclusively for your brand.
Built compliant.
Documented fully.
Every certification, every lab result, every record — ready for your US import, PMTA filing, and retail partners.
Indian FDA (CDSCO) Approved
Full pharmaceutical regulatory approval from India's CDSCO. Drug-manufacturing standards throughout every production run.
Quality Control & Documentation
Documented production processes, traceable batches, audit-ready records. Pharma-standard quality controls applied throughout every production run.
In-House Lab Testing
Our own laboratory tests every single batch — nicotine concentration, ingredient purity, and microbiological safety — before any shipment leaves our facility.
Pharma-Grade Ingredients
USP-standard pharmaceutical nicotine. Pharma-grade base material, sweeteners, and flavoring agents throughout. No food-grade shortcuts anywhere in our process.
CoA with Every Shipment
Certificate of Analysis, ingredient declarations, and manufacturing compliance records provided with every single order shipped.
PMTA Documentation Support
We produce all manufacturing documentation needed to support your US FDA PMTA filing process — CoA, batch records, ingredient lists.
US Labeling Compliance
FDA-mandated nicotine addiction warning and Tobacco 21 (21+) age restriction labeling incorporated into all packaging we produce.
Legal Export Manufacturing
Manufacturing nicotine products exclusively for export is fully legal under Indian law. COTPA domestic-sale restrictions do not apply to export production. We operate under CDSCO pharma licensing — India's FDA equivalent — with pharma-grade quality standards throughout.
Important US Compliance Information
We are transparent about what brand owners need to know before launching in the US market.
- Nicotine pouches are regulated as tobacco products by the US FDA. Brand owners importing or selling in the US may require a Premarket Tobacco Application (PMTA). We strongly recommend a qualified US regulatory attorney before launch.
- All US nicotine products must carry: "WARNING: This product contains nicotine. Nicotine is an addictive chemical." We provide labeling guidance and incorporate compliant warnings into all packaging.
- Federal Tobacco 21 (T21) law restricts nicotine product sales to adults 21+ only. Age verification is the brand owner's and retailer's legal responsibility.
- Individual US states may impose additional restrictions, excise taxes, and retail licensing. Brand owners are responsible for state-level compliance in every market they enter.
- We provide CoA, ingredient declarations, manufacturing records, and export compliance documentation with every shipment to support your regulatory obligations.
- Our manufacturing is conducted under full CDSCO (Indian FDA) pharmaceutical licensing. India's COTPA regulations govern domestic nicotine product sales only — they do not apply to export manufacturing. This facility is legally compliant under Indian law for all export operations.
Where to find us.
We attend the top US industry trade shows in person. Stop by the booth, see samples, ask questions, and meet Aman face-to-face before signing your first order.
TPE 2026
Total Product Expo — the premier US trade show for tobacco alternatives, vape, and convenience retail. We met with US distributors, retailers, and brand owners exploring the white label and private label pouch opportunity.
CHAMPS Las Vegas
CHAMPS Trade Show — the largest B2B counter-culture and smoke-shop expo in the United States. Strong networking with smoke shop chains, distributors, and emerging pouch brands looking for a manufacturing partner.
CHAMPS Chicago
Join us at CHAMPS Chicago — the Midwest's leading B2B trade show for the alternative tobacco and wellness category. Book a meeting in advance to walk through pricing, samples, and timelines for your white label or private label launch.
Lock in a 30-minute booth meeting with Aman.
Questions answered
North America's bridge to
India's best pouch manufacturing.
We built PouchWhiteLabel to give US brands a dedicated North American partner — pharma-grade pouch manufacturing with American-time-zone service and full accountability on every can shipped.
Toronto-based · North American operations
Your single point of contact on this continent. WhatsApp, call, or email — Eastern Time. No 12-hour delays, no language barriers, no time zone roulette.
Pharma-grade manufacturing
CDSCO-approved, pharma-grade facility producing for the US market since 2018. Pharmaceutical quality standards on every batch — not food-grade, not industrial-grade.
Direct production oversight
Our quality team coordinates from formulation through shipment for every US client. You get full visibility into your order at every stage — sampling, production, lab testing, and dispatch.