# FDA recall D-1319-2014

> **Flawless Beauty LLC** · Class II · drug recall initiated 2014-04-29.

## Product

Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable solution, 1500 mg/500 mg, packaged in 8-count vials, 8-count 5 mL vitamin C (ascorbic acid) solution diluent ampoules, and 30-count Advanced Glutathione Boosters capsules per box, Relumins Labs, 183 Locust Avenue, West Long Branch, NJ 07764, UPC 700175760302

## Reason for recall

Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling indicates it is to be used parenterally for drug claims.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1319-2014
- **Recalling firm:** Flawless Beauty LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Completed
- **Initiation date:** 2014-04-29
- **Report date:** 2014-05-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Asbury Park, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1319-2014

## Citation

> AI Analytics. FDA recall D-1319-2014. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-1319-2014. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
