Technical judgment
Blood orange may bring peel bitterness and a deep-color expectation. Black tea can intensify bitterness and dryness.
| Brand Name | OEM brand, ZhenXi |
| Certification | FDA, FSSC, GMP, HACCP, HALAL, ISO, |
| Delivery time | 20 – 25 days |
| Minimum Order Quantity | 2*20ft 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 · Five Elements Series
A 330ml Sleek canned concept combining a black tea direction with blood orange flavor for distributors, importers and beverage brands. ZhenXi reviews the formula, functional direction, process and packaging together before sampling or quotation.
Buyer decision summary
This page describes a product direction, not a globally fixed formula. The commercial version must be reviewed against ingredient documentation, destination-market classification, caffeine or taurine direction, sugar direction, carbonation, can specification and label requirements.
Product-specific information gain
Blood orange may bring peel bitterness and a deep-color expectation. Black tea can intensify bitterness and dryness.
ZhenXi separates peel note, fruit acidity and tea astringency during sample review and checks color stability.
The Sensory Scorecard and approved color reference become inputs to the batch-release specification.
Formula & sensory review
The sample review covers blood-orange aroma, citrus bitterness, black-tea body, sweetness, acidity, color and finish. Ingredient names alone do not define the finished drink: the same concept can change significantly with the tea system, flavor type, sweetener, acid balance, functional ingredients, processing and serving temperature.
| Review item | Decision required | Record |
|---|---|---|
| Ingredient identity | Flavor, extract, juice, powder or other documented input; no assumption from the product name | Ingredient specification / supplier documents |
| Functional direction | Caffeine, taurine, vitamins or other ingredients only after market and formula review | Formula Review |
| Sensory target | blood-orange aroma, citrus bitterness, black-tea body, sweetness, acidity, color and finish | Sensory Scorecard |
| Sample approval | Version, changes, comments and approval status | Sample Version Log |
| Claims | Only statements supported by the final product and destination-market rules | Artwork Review |
Packaging architecture
The final body format, end diameter and closure specification must be confirmed for the selected production line. A capacity name alone does not prove compatibility.
Tea, fruit-acid, botanical, mineral and carbonated systems require a compatibility review covering the liner, process, seam and planned shelf-life validation.
Printed can, sleeve or label route, carton configuration and pallet plan affect MOQ, artwork lead time and residual packaging risk.
These figures come from the supplied export packing reference dated 2024-01-07. They show planning quantities without pallets. Final loading must be reconfirmed against the approved carton, gross weight, pallet or floor-loading method, route restrictions and shipment plan.
| Carton configuration | Carton gross weight | Carton size | 20 ft container | 40 ft container | ||||
|---|---|---|---|---|---|---|---|---|
| Cartons | Cans | Gross weight | Cartons | Cans | Gross weight | |||
| 24 cans / carton, film-wrapped | 8.6 kg | 355 × 240 × 150 mm | 2,200 | 52,800 | 18,920 kg | 3,100 | 74,400 | 26,660 kg |
Planning boundary: container quantities are reference figures, not a guaranteed shipment count. Any palletized plan will use different quantities and must be calculated after the final packing specification is approved.
Approval workflow
Schedule is assessed from the actual critical path, which may include ingredient procurement, sample approval, formula confirmation, test data, artwork approval, can decoration, production planning and export documents. A generic lead time should not replace a project schedule.
QC & traceability
Applicable controls may cover incoming materials, batch weighing, blend attributes, fill level, can seam, leakage, sensory comparison, microbiological checks, coding, packaging and finished-product release. The approved specification determines the actual tests and acceptance criteria.
Finished product lot → production record → formula version → raw-material lots → packaging lots → release record.
Repeat orders should use the approved sample, retained sample, formula version and change-control record as references. An ingredient or supplier change should not be silently substituted.
Target-market coordination
Energy-drink classification, permitted ingredients, caffeine warnings, nutrition presentation, sugar claims, botanical naming and advertising evidence differ by market. ZhenXi can coordinate manufacturing information and artwork inputs based on the approved specification, but the brand owner should obtain final market-specific legal approval.
FAQ
ZhenXi first reviews the target market, formula status, ingredient documentation, intended blood orange direction, caffeine or taurine direction, sugar direction, carbonation requirement and 330ml Sleek can specification. A sample is a development version, not proof of regulatory or production approval.
ZhenXi separates peel note, fruit acidity and tea astringency during sample review and checks color stability. The Sensory Scorecard and approved color reference become inputs to the batch-release specification.
They may be reviewed for private label or custom-formula projects. Final ingredient selection and levels depend on documentation, target-market rules, sensory balance, process compatibility and the approved specification. ZhenXi does not treat every botanical or functional direction as automatically feasible.
MOQ is assessed by SKU count, flavor count, formula ingredients, 330ml Sleek can availability, print or sleeve route, carton configuration, changeover requirements and destination. It should be confirmed after the technical and packaging brief is complete rather than published as one universal number.
Artwork should be frozen only after the relevant formula version, ingredient declaration, nutrition data, required warnings and target-market review are sufficiently complete. The brand owner remains responsible for final legal approval in the destination market.
The approved sample, formula version, sensory reference and packaging specification become production inputs. Commercial batches are reviewed through incoming-material, blend, filling, seam, leak, sensory, microbiological and finished-product controls as applicable to the approved plan.
RFQ passport
Include target market, formula status, functional and caffeine direction, sugar direction, flavor and sensory target, carbonation, 330ml Sleek packaging preference, SKU count, estimated quantity per SKU, artwork status, destination and target schedule.