Magnesium citrate
118
labels across all brands · median 217.5 mg/serving
Brand · NIH DSLD
vitafusion magnesium labels
vitafusion files 1 on-market magnesium label; the magnesium salt is not named in the filed record for it, so the compound mass cannot be computed.
Labels (n)1
Median elemental mg/serving165 mg
Priced in gold set0
Composition across the portfolio · as filed
What vitafusion puts in the capsule besides magnesium
- 1 label uses a gelatin shell.
Label declarations · as filed
What vitafusion claims on its labels
Filed declarations across this brand's labels: 3 distinct filed entries across 1 NIH DSLD labels, counted 2026-09-13; these are manufacturer statements.
- Adult (18 - 50 Years) — on 1 of 1 label
- Gluten Free — on 1 of 1 label
- Dairy Free — on 1 of 1 label
What is not known · as of 2026-09-13
Gaps in the record for vitafusion
- 1 of 1 label does not name the magnesium salt in the filed record, so no compound mass can be computed for it.
- 1 of 1 label has no US retail listing matched as of 2026-09-13. That is a matching gap on our side, not evidence of unavailability.
Labels 1
| Magnesium 165 mg Adult Gummies Natural Tropical Citrus FlavorNIH DSLD · Label 246151 · Gummy or Jelly | citrate, oxide | 165 mg | 30 | 4.95 g | Not tracked yet |
Forms filed
Compare within a form
Magnesium oxide
108
labels across all brands · median 310 mg/serving
See all brands, all labels, or the priced form tables.
Filed composition facets
5 published excipient facets occur across 1 labels from vitafusion in the NIH DSLD records, counted 2026-09-13.
- citric acid: 1 of 1 labels.
- gelatin: 1 of 1 labels.
- glucose syrup: 1 of 1 labels.
- sugar: 1 of 1 labels.
- water: 1 of 1 labels.
FDA recall records for this firm
The FDA enforcement database holds 6 recall records naming vitafusion (queried 2026-09-13); 0 of them concern a magnesium product.
These are exact brand-string matches in the recalling-firm field or product description, including other products. A name match does not establish that two similarly named firms are the same legal entity. The recalling firm and recalled product are shown in each row.
| Report date | Class | Product described by FDA | Reason for recall | Status | openFDA record |
|---|---|---|---|---|---|
| 2021-05-05 | Class II | vitafusion Melatonin 140ct, 3 Pack 140 CT vitafusion Melatonin 44ct , 3Pack 44CT Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center. Description does not name a magnesium product. | Potential presence of a metallic mesh material in products. | Terminated | F-0464-2021 |
| 2021-05-05 | Class II | vitafusion Fiber Well 220ct, 10 / 220 CT Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center. Description does not name a magnesium product. | Potential presence of a metallic mesh material in products. | Terminated | F-0462-2021 |
| 2021-05-05 | Class II | vitafusion SleepWell 250ct / 24 / 250 CT Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center. Description does not name a magnesium product. | Potential presence of a metallic mesh material in products. | Terminated | F-0466-2021 |
| 2021-05-05 | Class II | vitafusion Fiber Well 90ct, 4/3 Pack 90CT Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center. Description does not name a magnesium product. | Potential presence of a metallic mesh material in products. | Terminated | F-0463-2021 |
| 2021-05-05 | Class II | vitafusion MultiVites 150ct, Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center. Description does not name a magnesium product. | Potential presence of a metallic mesh material in products. | Terminated | F-0461-2021 |
| 2021-05-05 | Class II | vitafusion Kids Melatonin 50ct, 4 / 3 PACK 50CT Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center. Description does not name a magnesium product. | Potential presence of a metallic mesh material in products. | Terminated | F-0465-2021 |
FDA assigns 3 recall classes by the assessed hazard, using the FDA classification definitions, checked 2026-09-13:
- Class I: Exposure to or use of the violating product carries a reasonable probability of serious harm to health or death.
- Class II: Exposure or use may produce temporary or medically reversible harm; the probability of serious harm is remote.
- Class III: Adverse health consequences from exposure or use are unlikely.
The FDA adverse event reporting system (CAERS) holds 66 reports naming vitafusion as of 2026-09-13. This is a count of submitted reports across all the firm's products; it is not an incidence rate and implies no causation.
The metric
What EC100 measures
EC100 = container price ÷ (elemental mg per serving × servings per container ÷ 100)
It normalizes the declared elemental amount to a 100 mg unit. It does not score ingredients, quality, or outcomes.