AI-generated product and packaging concepts for illustration only. Final appearance, dimensions and packaging must be confirmed with physical samples.
A skin-sensitivity reference formula with quercetin, bovine colostrum, spirulina, fish oil and a prebiotic and probiotic blend. The source specifies a chicken-flavored 2 g soft chew. Confirm ingredient sources and the proposed product wording before developing your private label version.
Species note: The catalogue describes dog and cat use; confirm the finished formula and serving directions for the intended species.
Use sample review to select piece size, shape and handling characteristics for the intended skin-sensitivity product. Neither a clean-looking chew nor a packaging design establishes a hypoallergenic formula. Keep appearance approval separate from ingredient-source and claim review.
AI-generated product and packaging concepts for illustration only. Final appearance, dimensions and packaging must be confirmed with physical samples.
The source names this an anti-allergy formula; this draft instead describes its composition and proposed skin-sensitivity positioning without making a prevention or treatment promise. Bovine colostrum, chicken flavor and fish oil are among the listed materials. Any exclusion claim or sensitivity-focused brief needs to be checked against the full ingredient specification.
| Active Ingredient | Reference Amount | Specification Note |
|---|---|---|
Fish oil |
40 mg | — |
Apple cider vinegar |
10 mg | — |
Brewer's yeast |
20 mg | — |
Prebiotic and probiotic blend |
12 mg | — |
Spirulina |
14 mg | — |
Quercetin |
8 mg | — |
Bovine colostrum |
6 mg | — |
Vitamin C |
8 mg | — |
Vitamin E |
6 IU | — |
Zinc |
4 mg | — |
Pea flour, Tapioca flour, Flaxseed, Natural chicken flavor, Carrot, Tomato, Glycerin, Phospholipids, Powdered cellulose, Potassium sorbate, Rosemary extract, Mixed tocopherols.
The ingredient table describes a reference composition, not a feeding schedule or a finished-batch assay. Confirm ingredient forms, the final formula version and species-specific directions before approving the product. The source grouping of active and base ingredients is retained; it is not a finalized label order.
Send us your destination market, target retail price and packaging idea. We come back with the route that fits: the reference formula as-is, an adjusted version, or a new formula built on the same chew base.
Values marked as reference come from the supplier formula sheet. Shape, dimensions and texture are only listed once confirmed with samples.
The reference pack is 2 g × 150 chews. The calculated net weight is 300 g; it is derived from the stated piece weight and count, not a test result. Shape, dimensions, texture limits and feeding directions require a confirmed product specification.
Start with this reference composition or submit a product brief for changes. For this formula, prioritize ingredient sources, the colostrum specification and the intended skin-positioning language. Formula, shape and weight customization are described in the catalogue; specific combinations remain subject to review.
Submit changes to the listed ingredients and define your requirements for ingredient sources, the colostrum specification and the intended skin-positioning language. A proposed change is not an already validated alternative formula.
Provide the target amount basis and intended daily serving. Revised ingredient levels should be recorded in a new formula version and reviewed with the chew specification.
The reference is 2 g per chew. The supplier describes a 0.5–3.5 g format range; confirm feasibility for this exact formula rather than applying the range to every product automatically.
Choose or request a shape for review against available tooling and the intended piece weight. Do not approve tooling or dimensional claims solely from a concept image.
The source lists chicken flavor. Alternative flavors and a specific texture target need review with the ingredients and sample; no unlisted flavor range is guaranteed here.
Confirm pack count, container, label and packaging sourcing. A different container or printed pack may involve a separate packaging minimum.
Reference shape options. Final shape is confirmed on the production mould.
Visual comparison only. Exact dimensions, gram weight and count are confirmed with samples.
AI-generated product and packaging concepts for illustration only. Final appearance, dimensions and packaging must be confirmed with physical samples.
Use a written formula version and sample reference when evaluating this product. Record the ingredient-amount basis, piece weight, appearance, selected shape, flavor, intended serving and pack details. Resolve ingredient sources, the colostrum specification and the intended skin-positioning language before treating the sample as the production reference. Any subsequent change should be captured in the revised specification.
The supplier reference is 500 bottles with 150 chews at 2 g each. Packaging may be sourced for the project or provided by you. Confirm product and packaging quantities together: custom printed materials follow the packaging supplier’s own minimum, and a change of formula or pack requires a revised quotation.
Reference Pack The listed reference is 150 chews at 2 g each. Confirm the bottle dimensions, closure, label area and final pack specification before artwork approval.
Supply Route The catalogue allows packaging to be sourced for the project or supplied by you. Custom packaging materials remain subject to their own supplier minimum quantities.
Review Required Submit a preferred pouch, jar or different pack count for review. These are project requests, not confirmed stocked options for every reference formula.
AI-generated product and packaging concepts for illustration only. Final appearance, dimensions and packaging must be confirmed with physical samples.
For this formula, request ingredient-source details for the bovine colostrum and flavor system, the probiotic blend specification and the basis of the zinc declaration. The agreed COA should identify actual tests, rather than repeating a general claim that the product is allergy-friendly.
Request confirmation of ingredient sources, the colostrum specification and the intended skin-positioning language. Preserve the approved ingredient identities and amount basis.
Confirm the applicable physical, microbiological and other test items, their limits and methods. This is a review scope, not a claim that every suggested test is performed on every batch.
Confirm the product and formula version, batch identification, COA scope and traceability documents available for the order.
Request the current product specification and available batch-document examples. The supplied reference catalogue mentions batch checks and COA support, but no SKU-specific COA or test report is attached here.
Share the destination country, intended species, proposed product name, label wording and serving directions before artwork approval. For this reference, include ingredient sources, the colostrum specification and the intended skin-positioning language in the review. The reference documents do not establish registration or acceptance in every market.
Discuss the required stability information for the final blend and its packaging, particularly any probiotic specification or other ingredient level that will be declared. No stable viable count, defined shelf life or after-opening period is supplied with this reference.
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Tell Arlo your target market and quantity. You receive a reference spec, a quote and a sample plan, and nothing moves to production until you have approved the sample.
No supporting assessment is provided. The listed materials include bovine colostrum, fish oil and natural chicken flavor. Their presence and sourcing need review against your specific exclusion brief; the source product name alone does not substantiate a hypoallergenic claim.
The reference lists 8 mg quercetin and 6 mg bovine colostrum per 2 g chew. It does not specify quercetin raw-material purity or colostrum standardization. Request those specifications before treating the listed ingredient weights as a defined marker-compound claim.
The source lists 12 mg of a prebiotic and probiotic blend without strains or a CFU value. No numerical viable-count declaration can be derived from that mass entry. Confirm the product-specific blend and the basis for any count claim.
Submit the ingredients and flavor sources you need to exclude. A replacement is a formula change that requires ingredient-source and sample review. The supplied documents do not identify a ready chicken-free version of this particular formula.
The base lists potassium sorbate, along with mixed tocopherols and rosemary extract. Do not describe this reference as preservative-free by default. Review the complete declaration and the applicable wording for the intended market.
Not without review. The supplied files provide a formula and marketing description, not evidence supporting an allergy-prevention or treatment claim. The proposed use and wording should be assessed for the destination market before the public name is approved.
The supplier describes formula, shape and piece-weight customization. The 0.5–3.5 g range is a range-level capability, not confirmation that this exact formula is available at every weight. For this product, submit your targets for ingredient sources, the colostrum specification and the intended skin-positioning language before a revised sample specification is agreed.
The source lists 500 bottles for a 2 g × 150-chew reference pack. It separately states that custom packaging is subject to the packaging supplier’s minimum. Confirm the selected formula, pack count and packaging requirements together; do not interpret 500 bottles as an unconditional minimum for every printed container.
Approve a written formula version and specification alongside the sample. Include the ingredient-amount basis, piece weight, appearance, intended serving and packaging details, with particular attention to ingredient sources, the colostrum specification and the intended skin-positioning language. Changes after approval should be recorded in a revised specification rather than handled only in informal messages.
Request the final product specification, the actual scope of the batch COA, and stability information linked to the formula and packaging you select. The supplied reference documents do not include a complete COA or stability study for this SKU, so no test results or fixed shelf-life period have been invented for this page.