Accreditation document
CNAS Accreditation
Review the holder and scope shown in the supplied accreditation document.
Company information & product documentation
Manufacturing Quality& Documentation.
Review manufacturing credentials, US/UK/EU label support and the export documents for your oral pouch or ODF order.
Oral pouches & oral dissolving films for brands and distributors.
01 / Company & credentials
Know your manufacturing partner.
ZestDose supports private label oral pouches and oral dissolving films for brands, distributors and importers. Review the company and product records for your selected market and order.
See completed customer product and packaging projects.
Manufacturing credentials
GMP / cGMPHACCPISO 22000FSSC 22000FDA
Applicable system and facility registration documents are confirmed for the relevant production site, product and destination.
Company information for your order
Confirm the contracting entity, business contact, official PI and corporate bank instructions before placing your order.
400,000cans/day
Oral pouch production capacity
Oral pouch production capacity
Pullulan & HPMCODF casting
4-layer foil sachet options
4-layer foil sachet options
29Countries served
US, UK, EU & global markets
US, UK, EU & global markets
35Brands served
Brand and distributor projects
Brand and distributor projects
Supplied documents
Certificates & registration documents.
View the supplied files in full. Documents apply to the holders, scopes and periods stated in each file.
Facility registration document
FDA Registration Documentation
Review the facility information in the supplied registration document.
02 / Quality & export records
Documents for your product.
Confirm the quality, export and carrier records for the agreed product, route and destination.
Company & Order Records
- Contracting entity details
- Official Proforma Invoice (PI)
- PI-confirmed corporate bank instructions
Facility Credentials
- GMP / cGMP & HACCP records
- FSSC 22000 & ISO 22000:2018
- US FDA food facility registration
Pre-Shipment Batch QC
- Batch Certificate of Analysis (COA)
- Product Specification Sheet
- Factory Inspection Report
Customs & Transport Pack
- MSDS / SDS (Safety Data Sheet)
- Applicable air / sea transport assessment
- Commercial invoice & packing list
- Export inspection records, where required
Choosing finished cartons? Review our in-stock oral strips before requesting product-specific documents.
03 / Labels, brand & destination
Confirm your product, brand & market.
Agree the market requirements, brand records and packaging brief before formula and artwork approval.
Destination & country-specific ingredient limits
Confirm the exact destination before finalizing the formula. Ingredient eligibility, ingredient form, amounts per serving and daily intake requirements can differ by country. For Spain and other EU destinations, review the applicable composition and labeling rules before sampling or printing. The agreed specification records the workable formula for that market.
US FDA, UK & EU label support
Our label-support team helps adapt artwork for US, UK and EU projects. For U.S. products, review the applicable product identity, Supplement Facts or other required information, net quantity, ingredient declarations and warnings against the agreed classification. For the UK and EU, confirm the jurisdiction, language, responsible business details and permitted claims before artwork approval.
Trademark application receipts (™) & export records
If your trademark application is pending, send the application receipt and brand authorization details for project review. Use ™ and registered symbols according to the applicable rights; an application receipt alone does not establish non-infringement or guarantee clearance. DDP and other delivery terms do not remove origin export obligations. We coordinate applicable declarations, inspections and records with the exporter and broker.
Sales channel, barcodes & importer coordination
Tell us whether you sell through Amazon, TikTok, retail or pharmacy chains, or regional distribution. We support applying your approved UPC/EAN and Amazon FNSKU codes and agreed carton labels. Confirm your importer or broker, forwarder requirements and channel-specific document checklist before packaging and dispatch.
Sample approval, artwork changes and project responsibilities are explained in our Wholesale & OEM Policy.
04 / Freight & report coordination
Your forwarder or ours.
For the agreed shipment, we coordinate the batch COA and applicable MSDS/SDS and transport assessment alongside the commercial invoice and packing list. Confirm the required document set before booking.
ZestDose's forwarding partners — DDP / CFR
Request DDP delivery to a named destination where available, or CFR/CIF for suitable sea freight. DDP includes the agreed import clearance and applicable duties and taxes; CFR/CIF responsibilities are stated separately on the quote. Existing MSDS and transport reports can be used when they cover your actual product and packaging and are accepted by the booked carrier.
Your nominated forwarder — EXW / agreed handover
Share your forwarder's checklist before dispatch. Confirm the applicable EXW, FOB or other agreed delivery term. If the carrier requires reports for the exact product name, specification or consignor, the MSDS and transport assessment must be prepared or updated to match those requirements.
See the Shipping Policy for dispatch and transit terms. The Payment Policy explains order and pre-shipment milestones.
05 / Buyer questions
Questions before you order.
Start with your product, destination and document requirements.
Which quality and export documents do you provide?
Commercial orders are supported by a batch COA, Product Specification Sheet and Factory Inspection Report. Applicable facility credentials include GMP/cGMP, FSSC 22000, ISO 22000, HACCP and US FDA food facility registration. We also coordinate MSDS/SDS and transport assessments for the agreed product, carrier and destination.
Can your team help adapt labels for US FDA, UK and EU requirements?
Yes. Our label-support team reviews the applicable product classification, ingredient information and packaging text for US, UK and EU projects. U.S. artwork is prepared with the applicable FDA label requirements in view; UK and EU jurisdiction, language and responsible business information are confirmed for the destination before printing.
Can we provide a trademark application receipt while registration is pending?
Yes. Send the application receipt and brand ownership or authorization information for project review. The ™ symbol does not mean the trademark is registered, and a receipt does not by itself establish non-infringement or guarantee clearance. Applicable origin export requirements still need to be met when DDP delivery is used.
How do MSDS and transport reports differ with your forwarder and ours?
With our forwarding partners, existing MSDS and transport assessments can be used when they cover the actual goods and packaging and are accepted for the booked transport. Your nominated forwarder may require reports under the exact product name, specification or consignor. Share its checklist early so applicable product-specific records can be coordinated.
Why confirm the exact destination before finalizing the formula?
Ingredient eligibility and permitted amounts depend on the product and country. Spain and other European destinations may have additional national requirements. Confirm the destination, ingredient forms, serving amounts and daily intake before sampling or printing so the applicable formula and label requirements can be reviewed.
How are DDP or CFR freight quotes calculated?
Send Cara the product, box or can quantity and destination postcode. The quote considers the packed weight, carton dimensions, route and delivery service. DDP quotes identify the named destination and import clearance and duty/tax scope. CFR quotes identify the destination port and the applicable sea-freight responsibilities.
