AI-generated product and packaging concepts for illustration only. Final appearance, dimensions and packaging must be confirmed with physical samples.
A respiratory-positioned reference formula with licorice, thyme, honey, lysine and additional botanical ingredients. The source lists a chicken-flavored 2 g soft chew. Confirm ingredient identities, intended species and product classification before proceeding with a private label brief.
Species note: The catalogue describes dog and cat use; confirm the finished formula and serving directions for the intended species.
Review the selected chew and packaging presentation after the ingredient identities and intended product use are defined. Images should describe physical presentation only, without symptom graphics or implied proof that the product treats a respiratory condition.
AI-generated product and packaging concepts for illustration only. Final appearance, dimensions and packaging must be confirmed with physical samples.
The supplier describes this as a respiratory-support formula. Its quotation lists multiple botanicals in both the active table and the base, together with a digestive enzyme blend. The documents do not establish treatment of coughs, infections or other respiratory conditions. This composition should be reviewed as a specific formula, not accepted on the strength of the category name alone.
| Active Ingredient | Reference Amount | Specification Note |
|---|---|---|
Fish oil |
30 mg | — |
Brewer's yeast powder |
20 mg | — |
Licorice powder |
10 mg | — |
Hollyhock root powder |
10 mg | Confirm botanical identity; do not silently substitute marshmallow root. |
Thyme |
10 mg | — |
Digestive enzyme blend |
40 mg | — |
Honey |
8 mg | — |
Chinese skullcap |
6 mg | — |
Lysine |
6 mg | — |
Vitamin E |
5 IU | — |
Vitamin B2 |
2 mg | — |
Vitamin C |
9 mg | — |
Chickpea flour, Pea flour, Natural chicken flavor, Mixed tocopherols, Loquat leaf powder, Mulberry root bark, Rosemary extract, Powdered cellulose, Glycerin, Phospholipids.
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 botanical identities, ingredient forms and the intended respiratory positioning. 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 botanical identities, ingredient forms and the intended respiratory positioning. 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 botanical identities, ingredient forms and the intended respiratory positioning 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.
Request complete botanical specifications, including plant identity and part, and clarification of the enzyme blend's identity and activity. The formula contains a root-powder name that needs confirmation before translation into a final ingredient declaration. No respiratory efficacy report is provided with this reference.
Request confirmation of botanical identities, ingredient forms and the intended respiratory positioning. 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 botanical identities, ingredient forms and the intended respiratory positioning in the review. The reference documents do not establish registration or acceptance in every market.
Ask for stability information corresponding to the actual botanicals, enzyme blend and packaging that will be used. Define the storage claim only after the product specification and available evidence have been reviewed. No numerical shelf life is assigned to 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.
The active table includes licorice powder, a root powder named 蜀葵根粉, thyme and Chinese skullcap. The base includes loquat leaf powder and mulberry root bark. Exact botanical identities, material forms and applicable specifications should be confirmed before final labeling.
The source says 蜀葵根粉, which is retained in the source record and provisionally translated as hollyhock root powder. It should not silently be changed to marshmallow root. Confirm the botanical name and plant part with the supplier.
The table lists 40 mg of digestive enzyme blend per 2 g chew but provides no enzyme identities or activity units. Ask for those specifications before determining whether the blend matches your proposed product requirements.
No such evidence is supplied in the two source files. The catalogue includes broad respiratory claims, but a formula list does not establish treatment performance. The intended use and wording require separate review before publication.
Not consistently. Several ingredients are named as powders or whole botanical materials, without extract ratios or marker concentrations. Keep those forms distinct and request clarification rather than describing every botanical as a concentrated extract.
No market approval or species-specific use file is supplied here. The catalogue describes both species, but that does not establish approval for your intended country or label. Provide the destination and complete product brief before finalizing the project.
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 botanical identities, ingredient forms and the intended respiratory positioning 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 botanical identities, ingredient forms and the intended respiratory positioning. 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.