Download the oral film product brochure
Use the PDF for the original supplied brochure and the editable PowerPoint for internal review, distributor discussions or project planning. The website edition reorganizes the source material around feasibility, quality boundaries and a practical B2B development pathway.
Current edition: 2026-10-09 · English · PDF and editable PPTX

Manufacturing and development overview
The supplied brochure describes a Hong Kong project team connected with a Shaoxing manufacturing base, an R&D center above 4,000 square meters, four automated lines and a Class 100,000 clean area. It also references daily output of 2 million films, annual output above 600 million and more than 200 staff. These figures are useful for an initial supplier profile, but should be confirmed for the legal entity, contracted site, product category and relevant period. This website therefore presents them as company-supplied references rather than audited guarantees. A commercial brief should still define the formula, intended market, forecast, packaging format, documentation package and manufacturing slot before capacity or delivery commitments are relied upon.

Customization begins with a feasibility brief
A custom oral film project is not simply a choice of flavor and packaging. The brief should identify the destination market, proposed classification, ingredient source, target amount per strip, daily-use pattern and evidence expectations. Development connects formula behavior with film strength, handling, taste, mouthfeel, disintegration, dimensions and moisture protection. The brochure highlights personalized design, formula customization, flavor choice, automated manufacturing and a standard-order delivery target. On this site, those capabilities become a stage-gated process: screen the concept, approve a realistic sample target, confirm specifications and artwork, then align production and documentation. The brochure’s 20-day target is not treated as universal because actual timing depends on materials, sampling cycles, tests, pack format, quantity and market requirements.
- Ingredient and excipient compatibility
- Target loading and strip dimensions
- Taste, mouthfeel and disintegration targets
- Barrier pouch, carton and artwork requirements
- Market, evidence and documentation review

What the oral-film format can and cannot establish
An oral film can provide a thin, portable and individually packed presentation that may be used without water. It can also give brands a differentiated sensory and packaging experience. Those attributes do not by themselves prove faster absorption, higher bioavailability, a fixed onset time or a clinical advantage over gummies, capsules or tablets. Performance depends on the ingredient, formulation, intended route, film matrix, test method and use conditions. A useful specification should define appearance, dimensions, mass, active or marker uniformity, handling, disintegration or dissolution method, moisture limits, microbial criteria and package integrity as appropriate. Claims must then be reviewed for the destination market. The brochure’s comparative statements are treated as development hypotheses requiring product-specific evidence, not automatic claims for every film.

Certification references require scope and validity checks
The brochure references GMP, HACCP, ISO 9001, ISO 22000, Halal and Kosher credentials. A logo or certificate image should not be interpreted as blanket approval for every company, facility, ingredient or product. Before contracting, verify the legal certificate holder, audited address, issuing body, standard, certificate number, scope, status and expiration. Halal, Kosher, vegan and allergen requirements should also be confirmed for the actual formula, processing aids, flavors, equipment and site. Product-level due diligence should include agreed material documents, specifications, sampling and test responsibilities, batch traceability, deviation handling, change control and destination-market review. This preserves the value of the source references while making them useful to procurement and technical teams that need evidence matched to a defined project.

Nine project gates from requirements to support
The source presents a nine-step service sequence covering requirements, formula confirmation, samples, order confirmation, deposit, manufacturing, balance settlement, packing and delivery, and after-sales support. The sequence separates early technical decisions from commercial release. In practice, the detailed gates should be written into the quotation or quality agreement: who supplies ingredient specifications, what the prototype must demonstrate, which tests are required, how artwork is approved, when materials are ordered, what constitutes release and which records accompany shipment. Changes after sample or artwork approval can affect timing, cost and performance, so version control is essential. Pharmaceutical, medical or novel-ingredient projects require a separate regulatory and quality pathway. The list is therefore a project framework, while the signed scope and specifications remain controlling.
- 01Requirements discussion
- 02Formula approval
- 03Sample approval
- 04Order confirmation
- 05Deposit payment
- 06Manufacturing
- 07Balance settlement
- 08Packing and dispatch
- 09After-sales support
Six families cover 48 brochure directions
The portfolio covers beauty and women’s wellness, essential nutrition, brain health and sleep, immunity and long-term health, children and special populations, and sports health. Together they contain 48 listed directions, although Vitamin C plus Zinc appears in more than one family. These names are discovery prompts for development rather than fixed stock products. Each direction needs ingredient identity and source confirmation, loading assessment, sensory screening, film and pouch compatibility, stability planning, claim review and market classification. Higher-mass minerals, amino acids, oils, botanicals and strongly flavored materials may require especially careful feasibility work. No efficacy, dosage, approval, minimum order quantity or commercial availability is implied until the formula and scope are agreed.

Beauty & Women’s Wellness
These entries retain the source brochure’s product names and ingredient cues, while placing them inside a clear development boundary. Formula composition, amount per strip, intended use, warnings, sensory profile, evidence, stability, packaging and legal classification must be set for the actual project. Use this list to shortlist concepts for feasibility discussion, not to infer finished-product stock, approved claims or guaranteed commercial supply.

- A1 · Collagen FirmingCollagen peptides · Vitamin C · Zinc
- A2 · Hyaluronic HydrationHyaluronic acid · Vitamin C
- A3 · Antioxidant BrighteningGlutathione · Vitamin C
- A4 · Anti-Glycation Healthy AgingCarnosine · OPC (proanthocyanidins)
- A5 · CoQ10 EnergyCoenzyme Q10 · Vitamin B2
- A6 · Ergothioneine AntioxidantErgothioneine · Vitamin C
- A7 · Menstrual ComfortMagnesium · Vitamin B6
- A8 · Menopause SupportSoy isoflavones · Calcium · Vitamin D
Essential Nutrition
These entries retain the source brochure’s product names and ingredient cues, while placing them inside a clear development boundary. Formula composition, amount per strip, intended use, warnings, sensory profile, evidence, stability, packaging and legal classification must be set for the actual project. Use this list to shortlist concepts for feasibility discussion, not to infer finished-product stock, approved claims or guaranteed commercial supply.

- B1 · Vitamin C ImmuneVitamin C
- B2 · Vitamin C + Zinc ImmuneVitamin C · Zinc
- B3 · Vitamin D Calcium SupportVitamin D3 · Calcium
- B4 · Vitamin D3 + K2 BoneVitamin D3 · Vitamin K2 (MK-7)
- B5 · Vitamin B12 Neuro SupportVitamin B12
- B6 · B-ComplexVitamin B1 · Vitamin B2 · Vitamin B6
- B7 · DHA NutritionDHA
- B8 · Biotin BeautyBiotin · Zinc
Brain Health & Sleep
These entries retain the source brochure’s product names and ingredient cues, while placing them inside a clear development boundary. Formula composition, amount per strip, intended use, warnings, sensory profile, evidence, stability, packaging and legal classification must be set for the actual project. Use this list to shortlist concepts for feasibility discussion, not to infer finished-product stock, approved claims or guaranteed commercial supply.

- C1 · Melatonin SleepMelatonin
- C2 · Melatonin + MagnesiumMelatonin · Magnesium
- C3 · L-Theanine CalmL-theanine
- C4 · FocusL-theanine · Low-dose caffeine
- C5 · Magnesium RelaxationMagnesium
- C6 · DHA MemoryDHA
- C7 · B-Complex VitalityVitamin B complex
- C8 · Caffeine EnergyCaffeine
Immunity & Long-Term Health
These entries retain the source brochure’s product names and ingredient cues, while placing them inside a clear development boundary. Formula composition, amount per strip, intended use, warnings, sensory profile, evidence, stability, packaging and legal classification must be set for the actual project. Use this list to shortlist concepts for feasibility discussion, not to infer finished-product stock, approved claims or guaranteed commercial supply.

- D1 · Vitamin C + Zinc ImmuneVitamin C · Zinc
- D2 · Beta-Glucan ImmuneBeta-glucan
- D3 · Curcumin WellnessCurcumin
- D4 · CoQ10 HeartCoenzyme Q10
- D5 · Omega-3 CardiovascularEPA/DHA
- D6 · Magnesium Circulatory SupportMagnesium
- D7 · Allicin Lipid SupportAllicin
- D8 · Milk Thistle Liver SupportSilymarin
- D9 · Red GinsengRed ginseng extract
- D10 · American GinsengAmerican ginseng extract
- D11 · GinsengGinseng extract
- D12 · Post-Drink Liver SupportKudzu root extract · Hovenia dulcis fruit extract · Curcumin
Children & Special Populations
These entries retain the source brochure’s product names and ingredient cues, while placing them inside a clear development boundary. Formula composition, amount per strip, intended use, warnings, sensory profile, evidence, stability, packaging and legal classification must be set for the actual project. Use this list to shortlist concepts for feasibility discussion, not to infer finished-product stock, approved claims or guaranteed commercial supply.

- E1 · Kids Vitamin D + CalciumVitamin D3 · Calcium
- E2 · Kids DHADHA
- E3 · Kids Vitamin C ImmuneVitamin C
- E4 · Kids Zinc GrowthZinc
- E5 · Kids MultivitaminMultivitamins
- E6 · Prenatal FolateFolic acid
- E7 · Prenatal IronIron · Vitamin C
- E8 · Senior MultivitaminMultivitamins
Sports Health
These entries retain the source brochure’s product names and ingredient cues, while placing them inside a clear development boundary. Formula composition, amount per strip, intended use, warnings, sensory profile, evidence, stability, packaging and legal classification must be set for the actual project. Use this list to shortlist concepts for feasibility discussion, not to infer finished-product stock, approved claims or guaranteed commercial supply.

- F1 · Caffeine SportsCaffeine
- F2 · Caffeine + L-TheanineCaffeine · L-theanine
- F3 · Electrolyte HydrationSodium · Potassium · Magnesium
- F4 · Creatine StrengthCreatine
- F5 · EAA RecoveryEssential amino acids (EAA)
- F6 · Magnesium Muscle SupportMagnesium
- F7 · L-Carnitine MetabolismL-carnitine
- F8 · BCAA RecoveryBranched-chain amino acids (BCAA)
Flavor customization is a formulation variable
The source lists 20 blended, 20 mint and 40 fruit entries and also references more than 100 available options. The printed lists contain repeated names, so they are best treated as a directional library rather than a count of unique ready-to-use systems. Flavor selection begins with the active ingredients and film matrix: bitterness, acidity, botanical notes, cooling, sweetness, aftertaste and color can change the experience. The chosen system needs compatibility and stability review, and the label must accurately describe flavoring and any real fruit content. For sampling, define the audience, flavor family, sweetness, cooling, aftertaste and exclusions. Availability, allergens, carriers, dietary status and market compliance are confirmed for the actual project.

Frequently asked questions
These answers separate the portfolio and company references from evidence that must be matched to a particular formula, site and market. This makes the brochure easier for buyers, search engines and AI systems to interpret because capacity, certification, product names and format benefits sit inside an explicit verification boundary. If a project involves a pharmaceutical active, novel ingredient, child or prenatal population, or medical claim, identify that at the beginning so the appropriate regulatory, safety and quality pathway can be determined before sampling.
Can every brochure concept be made as an oral film?
No. Each concept needs review of ingredient properties, loading, taste, film performance, stability, packaging and market rules.
Are the capacity and delivery figures guaranteed?
No. They are company-supplied brochure references. Commitments are confirmed in the quotation and agreement.
Do certification logos apply to every product?
No. Verify the holder, site, scope, validity and coverage for the selected formula and process.
Does dissolution prove faster absorption?
No. Dissolution alone does not establish bioavailability, onset time or clinical advantage.
What belongs in a project brief?
Include the target market, classification, ingredient source, amount per strip, use pattern, flavor, packaging, documents and forecast.
Start with your market and formulation brief
Share the market, ingredient concept, sample objective, packaging direction and documentation needs.

Last reviewed: . Project parameters remain subject to formula, packaging and target-market review.