Quantity per flavor and artwork
Separate grape from any other flavor; do not combine unrelated SKU quantities into one assumed MOQ.
| Brand Name | OEM brand, ZhenXi |
| Certification | FDA, FSSC, GMP, HACCP, HALAL, ISO, |
| Delivery time | 20 – 25 days |
| Minimum Order Quantity | 1 Container |
| Packaging | Can |
| Payment Options | L/C, T/T, Western Union, MoneyGram, Paypal |
| Place of Origin | China |
| Selling point | Fast, Fresh, Natural, Free Label Design, Private Label |
| Shelf Life | 12 Months Above |
| Volume | 330 ml(11.2 oz) |
OEM & Private Label Project Review
Evaluate a grape-led, carbonated low-alcohol beverage direction as a complete manufacturing system: alcohol base and classification, sensory target, 330ml can, artwork, production controls and destination-market requirements.
01 · Buyer Decision
“Hard seltzer” can describe different beverage bases and regulatory categories. Before sampling or quotation, the project needs a defined alcohol route, intended ABV, target market, formula status and packaging plan.
The technical review should connect each decision to an output: a product brief, sample version, approved specification, artwork review record or production assessment. If the product classification or alcohol base is still unclear, the correct status is subject to review—not production approved.
Recommended Image · 1600 × 1000 · 8:5
02 · Project Fit Matrix
This prevents sales copy, nutrition information and printed cans from getting ahead of the approved formula and market review.
| Decision Area | Current Page Basis | Required Factory Action | Release Evidence |
|---|---|---|---|
| Pack Format | 330ml canned product direction | Match can body, end, liner, filling and carton plan | Packaging specification |
| Grape Profile | Flavor direction only | Review aroma, sweetness, acidity, alcohol warmth, color and finish | Sensory scorecard |
| Alcohol Base & ABV | Not safely fixed for every project | Assess product route, target classification, process and label impact | Approved specification |
| Sugar / Natural Claims | No automatic claim | Check formula, evidence and destination-market thresholds | Label review record |
| MOQ & Schedule | Not one universal number | Calculate by SKU, formula, inputs, print route and production plan | Project quotation |
| Shelf Life | Must not be assumed | Define formula-specific validation and storage conditions | Validation basis |
Recommended Image · 1600 × 1000 · 8:5
03 · Formula & Sensory
A buyer needs more than a flavor name. The project brief should distinguish purple-grape, green-grape or other agreed direction, then connect that direction to sweetness, acidity, color, alcohol warmth and carbonation.
Coded versions can be reviewed as V1, V2 and V3. Each revision should record what changed and who approved it. The selected sample becomes a reference only after formula feasibility and scale-up considerations are checked.
04 · Approval Workflow
Each gate produces a decision or record. Submission of an inquiry is not formula approval, artwork approval or production approval.
05 · Can & Packaging Architecture
Capacity alone does not confirm compatibility. The selected body style, can end, internal liner, seam setup, pressure conditions, filling process, decoration route and carton must match the applicable site.
Recommended Image · 1600 × 1000 · 8:5
06 · Commercial Review
A reviewable quotation connects commercial terms to the actual technical scope. The same quantity may have different implications when the formula, alcohol base, can decoration, carton, SKU count or destination changes.
Separate grape from any other flavor; do not combine unrelated SKU quantities into one assumed MOQ.
Material route, order multiples and documentation can affect feasibility, cost and timing.
Artwork method changes print minimums, proofing steps, residual packaging risk and schedule.
Multiple formulas or packs can create additional setup, cleaning and approval requirements.
Pack-out and destination logistics must be confirmed before loading data is published.
The working schedule depends on when technical inputs and production files become approved.
07 · Existing Product Gallery
These existing product images can support recognition of the current offer. Add project-specific factory, sample-review, QC and packing evidence only when the applicable site and publication rights are confirmed.




Illustrative Workflow · Replace With Applicable Real Evidence
08 · QC & Batch Release
The applicable production site should define checks against the approved specification and process plan. Public copy should not invent tolerances, defect rates or laboratory results.
The decision is binary: release against the approved criteria, or hold for investigation. Marketing language must not replace the quality record.
09 · Target-Market & Label Review
The destination market, beverage basis and alcohol route can change product classification, mandatory statements, nutrition treatment, warnings, importer responsibilities and approval steps.
ZhenXi can coordinate available product and manufacturing information for artwork review. The brand owner and its qualified market adviser remain responsible for the final legal assessment and approvals. No single can label should be presented as “globally compliant.”
Recommended Image · 1600 × 1000 · 8:5
10 · Buyer FAQ
No fixed ABV is published for every project. The alcohol target must be reviewed with the beverage base, destination-market classification, sensory direction, process and label requirements before the specification is approved.
They can be reviewed as project directions. Coded samples should be compared for grape aroma, sweetness, acidity, alcohol warmth, carbonation, color and finish. A commercial formula is not frozen until the approved version and production fit are recorded.
No automatic sugar-free, no-added-sugar or natural claim is included. Any claim must match the approved formula, analytical or supplier evidence where required, and the rules of the destination market.
MOQ is reviewed per SKU and depends on formula mode, alcohol-base sourcing, can and decoration route, carton, ingredient purchasing, production changeover and destination requirements. It should be confirmed after the RFQ is technically reviewable.
Artwork should follow formula and classification review. The brand owner and its market adviser remain responsible for final legal approval, while production can coordinate available specifications, print files and manufacturing information.
Provide the target market, beverage classification, alcohol-base and ABV direction, formula status, grape sensory direction, sugar and carbonation direction, 330ml can requirements, SKU quantity, artwork status, destination and target schedule.
11 · RFQ Passport
A complete brief helps the team identify technical dependencies before it confirms sampling, commercial terms or a working schedule.