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Free Browser-Only Buyer Tool

Translate a gummy label target into formula-space arithmetic.

Enter one active target, its documented potency or assay basis, the serving architecture and proposed piece weight. The calculator shows the implied source-material mass and the arithmetic space left for everything else—it does not promise that the formula will deposit, set, dry, taste acceptable or remain stable.

Your entries and results stay in this browser. After a valid calculation, privacy-limited measurement may record only that this tool was used; it contains no ingredient, amount, potency, serving, adjustment, piece weight or result. Use non-confidential planning inputs only. Privacy notice.

Formula-Space Screen

Separate the label amount from the material mass.

Use the exact reporting basis from the supplier specification and proposed label. If potency, assay basis or source form is unknown, stop and obtain the document instead of inventing a percentage.

Folate: resolve label equivalents before entering milligrams

FDA describes folate on U.S. Nutrition and Supplement Facts labels in micrograms of dietary folate equivalents (mcg DFE). When folic acid is present, its amount is also stated in micrograms in parentheses. These label quantities are not the weight of a purchased premix. FDA label explanation.

Do not enter a mcg DFE number directly into Declared active target per serving (mg). Converting micrograms to milligrams alone does not resolve the equivalence basis. Before using this mass-based calculator, have the formulation and labeling reviewers reconcile:

  • The proposed folate label amount, unit and serving size, including any separately declared folic acid amount.
  • The exact folate form and supplier specification, including the assay/reporting basis and any carrier in the supplied material.
  • A documented constituent mass target and compatible material percentage for the calculator's inputs.

If that mapping is unresolved, leave the inputs blank and request clarification. The calculator does not convert DFE, validate a label, or establish finished-product potency, stability or manufacturing feasibility.

Buyer-entered planning basis

One material at a time. For a multi-active concept, repeat the screen and reconcile the combined material mass separately.

Use the proposed label basis for the named constituent—not the source powder mass.
Enter the applicable percentage from the material specification or COA basis.
Optional arithmetic scenario only. It is not an approved overage or label claim.
Use the proposed labeled serving count.
Finished piece mass, including the complete gummy matrix.
Source material / serving = declared active target ÷ (documented potency ÷ 100) × (1 + buyer-entered adjustment ÷ 100)
Source-material share = calculated source material ÷ proposed finished serving mass × 100
Interpretation Boundary

The percentage is a question generator, not a feasibility threshold.

01

Confirm the material basis

Identity, potency, carrier, moisture or dry basis and units must match the source document. A standardized constituent amount is not automatically the same as total source-material mass.

02

Budget the whole matrix

The arithmetic remainder must still accommodate the gelling system, water, sweetener, acid, flavors, colors, coatings, other actives and processing needs. It is not automatically usable capacity.

03

Test the proposed route

Mixing, transfer, depositing, setting, drying, release, texture, assay, package and stability evidence decide whether the proposed route is supportable. This tool does not evaluate those outcomes.

Three ingredient targets do not equal three powder weights

A gummy concept can look small when you add only the named constituent amounts. The physical material needed to deliver those amounts can be much larger. Before discussing how many actives fit in one serving, put every proposed material on a consistent mass and reporting basis.

The formula-space calculator handles one material at a time. For a multi-material concept, repeat that arithmetic and reconcile the total. This is a purchasing screen, not a recipe, intake recommendation or manufacturing feasibility result.

Start with documented inputs

For each material, identify the named constituent, its intended amount per serving, the supplier's stated constituent percentage and the basis on which that percentage is reported. Also identify whether two constituents come from the same material. A shared material should not be counted twice as though two separate powders will be added.

Do not substitute a generic percentage for an unknown specification. This mass-fraction worksheet does not convert CFU, enzyme activity, extract ratios or other non-mass units into milligrams. Those require a documented relationship appropriate to the specific material; an extract ratio alone is not a constituent assay percentage.

An intentionally fictional three-material example

The numbers below are invented solely to demonstrate mass balance. They are not recommended doses, approved overages, practical loading limits or descriptions of a Sucotond formulation. Assume three distinct non-overlapping source materials, matching reporting bases, and no planning adjustment.

Fictional three-material mass budget
Material Named constituent target per serving Hypothetical documented mass fraction Calculated source-material mass
A 250 mg 10% 2,500 mg
B 100 mg 20% 500 mg
C 10 mg 5% 200 mg
Total 360 mg of named constituents Not a combined assay 3,200 mg of source materials
Each source-material mass = its constituent target / its mass fraction
Total source-material mass = sum of the distinct source-material masses
Proposed serving mass = pieces per serving × finished piece mass
Material share = total source-material mass / proposed serving mass
Arithmetic remainder = proposed serving mass − total source-material mass

Suppose the proposed serving is two 3,000 mg pieces. The serving mass is 6,000 mg; the three materials account for 53.33%, leaving an arithmetic remainder of 2,800 mg per serving, or 1,400 mg per piece.

That remainder is not free manufacturing capacity. The worksheet does not calculate the gelling system, water, sweetener, acidity, flavor, color, coating or processing effects. It does not establish whether the materials can be mixed, deposited, set, dried or kept stable. A positive remainder is only an arithmetic observation.

Compare an alternative without claiming it will work

If the same fictional source-material total is distributed across three 3,000 mg pieces, the serving mass becomes 9,000 mg and the material share becomes 35.56%. That is a different serving architecture, not a validated formulation improvement.

At a fixed 60-piece bottle count, the change also reduces servings per bottle from 30 to 20. Carry that difference into the accepted-serving quote worksheet. Adding a piece can alter the commercial comparison even before any technical result is known.

The same targets with different hypothetical material fractions

Keep the fictional targets at 250 mg, 100 mg and 10 mg, but suppose three alternative unnamed materials have compatible mass fractions of 40%, 50% and 20%. The calculation changes as follows:

Alternative hypothetical material fractions
Alternative material Named constituent target Hypothetical mass fraction Calculated source-material mass
A2 250 mg 40% 625 mg
B2 100 mg 50% 200 mg
C2 10 mg 20% 50 mg
Total 360 mg Not a combined assay 875 mg

For the same two-piece, 6,000 mg serving, 875 mg is 14.58% of the mass, compared with 53.33% in the first calculation. Both calculations target the same named-constituent amounts; neither verifies delivered amounts or technical equivalence. The alternative fractions are invented, not evidence that such materials exist or are suitable substitutes.

Neither percentage is a manufacturing pass/fail threshold. Lower calculated mass does not prove an easier or feasible formulation. Use each scenario to ask what project-specific assessment is needed before interpreting a price as an offer for a manufacturable product. These unnamed-material exercises are separate from the magnesium RFQ case; do not infer its ingredient targets or an approved formula from them.

Reconciliation card for a project brief

Project mass-basis reconciliation
Check What to record Why an unresolved answer matters
Material identity Specification reference and version A generic ingredient name is not a controlled input
Constituent basis Named constituent, units, assay basis Unlike quantities should not be divided or added
Shared materials Which constituents belong to one source Prevents double-counting
Included carrier Whether the source-material specification already includes it Prevents adding the same carrier mass twice
Finished serving Piece count and proposed final piece mass Sets the denominator, not process capability
Adjustment Zero or a separately documented scenario Arithmetic adjustment is not an approved overage
Remaining questions Tests or decisions still needed A mass calculation does not answer stability or processing questions

If an assumed dry-basis assay is combined with an as-supplied material mass, stop and resolve the basis before presenting the result as comparable. Likewise, do not treat the finished-piece denominator as a manufacturing batch recipe; the worksheet has no process-water or drying model.

Protein gummy concepts: separate the protein target from powder mass

For a protein-gummy RFQ, first specify what the requested grams describe: source powder, protein supplied by that material, or protein measured in the finished serving. Those are different quantities. This is a concept-screening example, not confirmation that Sucotond offers a protein gummy or can deliver the proposed amount.

Supplier documents can report protein on different bases. For example, the Hilmar 9000 product bulletin has separate dry-basis and as-is protein rows, with typical values and specification limits in different columns. Its general data disclaimer also limits use of the bulletin as a guarantee. Obtain the current specification and appropriate lot evidence for the material actually proposed; this example is not a recommendation to buy that ingredient or proof of its performance in gummies.

The following values are fictional, not values copied from that bulletin or a customer project. Suppose a planning document gives 90% protein on a dry basis and 5% moisture by total as-supplied mass for the same material and compatible measurement basis:

As-supplied protein fraction = 0.90 × (1 − 0.05) = 0.855
For a hypothetical 8 g protein input target:
As-supplied powder mass = 8 / 0.855 = approximately 9.36 g
Using 90% directly would instead calculate 8 / 0.90 = approximately 8.89 g
Difference = approximately 0.47 g of source powder

This conversion assumes the two inputs describe the same material on compatible bases. Do not combine an unrelated typical moisture value with a protein minimum and call the result a batch assay. When the supplier provides a directly applicable as-is protein value, use its stated basis rather than correcting it for moisture a second time. The arithmetic assumes no protein loss and is not an overage recommendation, finished-product assay or shelf-life result.

Now perform a separate finished-serving sanity check. An invented 8 g protein target cannot fit inside two finished pieces weighing 3 g each: the entire serving weighs only 6 g. Three finished pieces weighing 4 g each total 12 g, so 8 g would represent 66.67% of finished serving mass. That avoids the simple mass contradiction, but does not establish an achievable texture, process or product.

Do not subtract the calculated 9.36 g of as-supplied powder from 12 g of finished gummies and label the remainder available formulation space. Input moisture and process losses require a batch mass balance; an incoming-material quantity and a final dried-piece quantity are not automatically comparable.

Before comparing OEM responses, record:

  • The requested protein source and whether any other ingredients also contribute protein. A total-protein result alone does not identify how much came from a particular source.
  • Protein amount per finished serving, piece count and intended final piece mass, with each unresolved input marked pending.
  • Source specification, reporting basis, moisture basis and which numbers are typical, limits or lot results.
  • Questions for the proposed trial: mixing and depositing behavior, final piece weight, texture, protein measurement, packaging and storage evidence. The worksheet does not answer these questions.
  • Which choices may change after assessment: amount, piece size, piece count or dosage format. More pieces also changes servings per container and the price comparison.

This is a procurement brief, not a determination that a consumer-facing "high protein" claim is permitted. Claim wording and finished-product measurement need their own applicable review.

Use the high-load project page and product specification checklist to organize the next questions.

Use the Output

Turn the arithmetic into a comparable manufacturer question.

Send the same basis to every supplier

  • Named material, form and supplier specification
  • Declared amount and reporting basis per serving
  • Documented potency or assay basis used in the screen
  • Proposed pieces per serving and finished piece weight
  • Other actives, dietary constraints, package and destination market
  • Which assumptions require bench, pilot or commercial-scale evidence

Do not use it as a dose or manufacturing promise

The calculator does not recommend an intake, approve an overage, determine legal labeling, account for every formulation component or establish commercial feasibility. Negative remaining mass means the entered arithmetic cannot fit inside the entered finished serving mass; a positive remainder does not prove manufacturability.

Build the controlled product specification · Plan sample-to-batch evidence

Sources and scope: 21 CFR 101.36 establishes that dietary-supplement labeling declares dietary ingredients and amounts per serving on the applicable basis. FDA's dietary-supplement cGMP guide frames specifications, production/process controls and testing as separate controls. Those sources support the need to preserve the label, material and production bases; neither source supplies a gummy-load threshold or validates a buyer-entered formula.

eCFR: 21 CFR 101.36, nutrition labeling of dietary supplements · FDA: dietary-supplement cGMP small-entity guide

Move from Arithmetic to Evidence

Share a non-confidential formula-space brief.

Bring the named material, source specification, label basis, serving architecture, package and target market. Sucotond USA can coordinate a project-specific feasibility review without treating this calculator as a production commitment.

Start a Formula-Space Review
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