ORALABX develops alcohol-free whitening mouthwash for established brands, importers and distributors. Peroxide-free development can be reviewed around a PAP-based system, with formula appearance, flavor, stability and packaging evaluated together. The approved formula and supporting test plan define the finished product specification and claim scope.
Home > Mouthwash OEM > MW03 Whitening Support Mouthwash
ISO-22716 Certified • GMP Manufacturing
MW03 Whitening Support Mouthwash
Minimum Order
10,000 units Lead Time
45–60 days
Whitening Support Mouthwash OEM Formulations/Specifications
Whitening Support Mouthwash OEM – Formula & Technical Parameters
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Product Type
Alcohol-free whitening mouthwash
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Formula System
Peroxide-free PAP-based development reviewed against the product brief; ingredient composition and levels confirmed in the approved formula.
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pH Specification
Formula-specific; recorded in the approved finished-product specification.
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Flavor Development
Mint or other agreed flavor direction, with sweetness, cooling and aftertaste adjusted during sampling.
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Packaging Format
Bottle volume, material, closure and dosing format confirmed through formula and packaging compatibility review.
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Minimum Order Quantity
Standard MOQ: 10,000 bottles per SKU. Custom packaging requirements are confirmed during quotation.
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Shelf Life
Established for the approved formula and packaging using stability and compatibility data.
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Quality & Documentation
Documented QC, batch traceability and project-specific technical documents. Relevant certificates available for qualified project evaluation.
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Lead Time
Typically 45–60 calendar days after formula, packaging, artwork and deposit confirmation. Custom tooling is scheduled separately.
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Packaging Customization
Private-label bottle decoration, labels and cartons, with closure compatibility and destination-market artwork reviewed before production.
Whitening Support Mouthwash OEM Features
Key Features of Whitening Support Mouthwash OEM
01
Whitening System Development
The whitening concept is translated into an agreed formula brief, with the test scope and intended claims defined before commercial approval.
02
Peroxide-Free Formula Direction
PAP-based options can be evaluated for peroxide-free positioning. The final ingredient declaration follows the approved formula.
03
Dispersion and Appearance Control
For suspended systems, particle distribution, settling behavior and redispersibility are evaluated during development.
04
Stability and Packaging Evaluation
Formula appearance and relevant quality parameters are reviewed alongside bottle and closure compatibility under the agreed test plan.
05
Flavor and Mouthfeel Adjustment
Mint intensity, sweetness, cooling and aftertaste are adjusted through sample evaluation against the brand brief.
06
Commercial Production Planning
Formula approval, packaging readiness, artwork confirmation and batch specifications are aligned before production scheduling.
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