Brand · NIH DSLD

New Age magnesium labels

New Age 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/serving70 mg
Priced in gold set0

Label declarations · as filed

What New Age claims on its labels

Filed declarations across this brand's labels: 1 distinct filed entries across 1 NIH DSLD labels, counted 2026-09-13; these are manufacturer statements.

What is not known · as of 2026-09-13

Gaps in the record for New Age

Labels 1

Labels
Magnesium GummiesNIH DSLD · Label 268743 · Gummy or Jellyform not mapped yet70 mg302.10 gNot tracked yet

Forms filed

Compare within a form

These labels file no magnesium form text (form not mapped yet).

See all brands, all labels, or the priced form tables.

Filed composition facets

5 published excipient facets occur across 1 labels from New Age in the NIH DSLD records, counted 2026-09-13.

FDA recall records for this firm

The FDA enforcement database holds 1 recall records naming New Age (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.

FDA enforcement records · queried 2026-09-13 · 1 records
Report dateClassProduct described by FDAReason for recallStatusopenFDA record
2014-01-08Class IINew Age Solutions Uri-Flow capsules packaged in a plastic bottle with 60 capsules per bottle.

Recalling firm: Mira Health Products Ltd.. Description does not name a magnesium product.

The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.TerminatedF-1298-2014

FDA assigns 3 recall classes by the assessed hazard, using the FDA classification definitions, checked 2026-09-13:

Full FDA record register and matching method →

The FDA adverse event reporting system (CAERS) holds 3 reports naming New Age 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.