Rainbow Light
Arthx Relief
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
2
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.
Supplement Facts
9 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitamin C UNII · PQ6CK8PD0R | 60 mg | 100% |
| Manganese UNII · 42Z2K6ZL8P | 4 mg | 200% |
| Molybdenum UNII · 81AH48963U | 150 mcg | 200% |
| Sodium UNII · 9NEZ333N27 | 110 mg | 4% |
| Glucosamine Glucosamine (unspecified)UNII · N08U5BOQ1K | 1500 mg | — |
| Chondroitin Chondroitin (unspecified)UNII · V5E8ELO4W9 | 1200 mg | — |
| Methylsulfonylmethane UNII · 9H4PO4Z4FT | 100 mg | — |
| Boron Glycinate BoronUNII · YV58Q9ER5F | 1.5 mg | — |
| Soothing Blend Blend (Combination) | 0 NP | — |
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.
- from: Vitamin C
- from: Vitamin C
- from: Vitamin C
- from: Manganese
- from: Manganese
- from: Molybdenum
- from: Vitamin C
- from: Vitamin C
Flagged excipients
1 flagged · authority citations
- ● AVOIDTitanium Dioxidecolor
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.
FDA CAERS · adverse event context
2
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
Stearic Acid · Cellulose · Hypromellose · Polydextrose · Talc · Maltodextrin · MCT · Riboflavin