Mason Natural

Calcium 600 + D3 400 IU

Serving

1 Tablet(s)

Form

tablet

UPC

311845088918

DSLD

240011

Formula hash

141de3521578

Brand context

Mason Natural

Catalog

249

products

With avoid flag

products

FDA recalls

history

CAERS

reports

Avoid-flaggedObjective label signals

Flagged excipients

1 avoid · 1 caution

FDA recalls

no recall history

CAERS reports

FDA consumer events

Certifications

none recorded

1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

2 active ingredients

Ingredient	Amount	% DV
Vitamin D3 Vitamin DvitaminUNII · 1C6V77QF41 UL · set4 effects	400 IU	100%
Calcium mineralUNII · SY7Q814VUP UL · set6 effects	600 mg	60%

What this product supports · authorized claims

8 authority-backed effects

Rolled up from EFSA / FDA / NIH ODS authorized function claims on this product's active ingredients. Each row shows which ingredients contribute.

↑Maintenance of normal bones
from: Calcium · Vitamin D
EFSAEU-Reg-432/2012-ID-228 →
↑Normal muscle function
from: Calcium · Vitamin D
EFSAEU-Reg-432/2012-ID-226 →
↑Normal blood coagulation
from: Calcium
EFSAEU-Reg-432/2012-ID-227 →
↑Normal energy-yielding metabolism
from: Calcium
EFSAEU-Reg-432/2012-ID-234 →
↑Normal function of digestive enzymes
from: Calcium
EFSAEU-Reg-432/2012-ID-355 →
↑Role in the process of cell division
from: Calcium
EFSAEU-Reg-432/2012-ID-237 →
↑Calcium absorption
from: Vitamin D
EFSAEU-Reg-432/2012-ID-152 →
↑Normal immune system function
from: Vitamin D
EFSAEU-Reg-432/2012-ID-154 →

Flagged excipients

2 flagged · authority citations

● AVOIDTitanium Dioxide
color
Banned in EU food products effective 2022-08 (Commission Regulation (EU) 2022/63) following EFSA Panel opinion that a safe daily intake could not be established due to genotoxicity concerns. Still GRAS in the US under 21 CFR 73.575 but EU position is stricter.
eur-lex.europa.eu →efsa.europa.eu →ecfr.gov →
◐ CAUTIONFD&C Yellow #6 Lake
color
EU requires 'attention in children' warning per Reg 1333/2008 Annex III (Southampton study 2007). Banned in Norway + Finland; allowed in US under 21 CFR 74.706 with declaration.
eur-lex.europa.eu →

FDA CAERS · adverse event context

consumer-submitted adverse event reports filed with the FDA CFSAN Adverse Event Reporting System mentioning this product or its brand.

CAERS reports are unverified consumer submissions — not adjudicated causality. Large well-known brands accumulate proportionally more reports simply due to broader use. About CAERS →

Other ingredients

Acacia · Maltodextrin · Croscarmellose Sodium · Microcrystaline Cellulose · Hypromellose · Soy Polysaccharides · Sodium Lauryl Sulfate · Magnesium Sulfate · Triacetin · Mineral Oil

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.