Country Life

Arthro-Joint & Muscle Support Factors

Serving

3 Softgel(s)

Per container

Form

capsule-unknown

UPC

015794049838

DSLD

14167

Avoid-flaggedObjective label signals

Flagged excipients

1 avoid · 0 caution

FDA recalls

1 Class I / II

CAERS reports

FDA consumer events

Certifications

none recorded

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

Supplement Facts

16 active ingredients

Ingredient	Amount	% DV
Calories UNII · 1	25 {Calories}	—
Total Fat Fat (unspecified)	2 g	3%
Protein Protein (unspecified)	1 g	2%
Vitamin C UNII · PQ6CK8PD0R	50 mg	83%
Vitamin E UNII · H4N855PNZ1	25 IU	83%
Manganese UNII · 42Z2K6ZL8P	5 mg	250%
Boswellia serrata extract BoswelliaUNII · 4PW41QCO2M	500 mg	—
Omega-3 Fish Oil Concentrate Fish Oil	400 mg	—
Glucosamine Glucosamine (unspecified)UNII · N08U5BOQ1K	200 mg	—
Chondroitin Sulfate UNII · V5E8ELO4W9	200 mg	—
Glucosamine Glucosamine (unspecified)UNII · N08U5BOQ1K	125 mg	—
Poly-NAG N-Acetyl Glucosamine	50 mg	—
Green Lipped Mussel extract New Zealand green-lipped mussel	50 mg	—
Cetyl Myristoleate UNII · 87P8K33Q5X	50 mg	—
Gamma-Linolenic Acid Gamma Linolenic AcidUNII · 78YC2MAX4O	50 mg	—
Boron UNII · N9E3X5056Q	1.5 mg	—

Flagged excipients

1 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 →

Recall history

1 FDA recall

Class II2014-06-19brand-level
Country Life TARGET MINS CALCIUM MAGNESIUM With Vitamin D3 Complex, WILD BLUEBERRY FLAVOR, LIQUID Dietary Supplement, 16 FL. OZ. (1 PINT) (472 mL), Product No. 2523, Bar Code 015794025238, and 32 FL. OZ. (1 QT) (944 mL), Product No. 2522, Bar code 015794025221 --- Manufactured for Country Life, LLC 180 Vanderbilt Motor Parkway, Hauppauge, NY 11788
Reason: The affected lots do not meet quality standards due to insoluble particulates.
FDA record →

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

Soybean Oil · Gelatin · Glycerin · purified Water · beeswax · Sunflower Lecithin · carob