ChingChunBao Anti-Aging Tablets Recalled for Unapproved Drug Claims
Murray International Trading Co. is recalling ChingChunBao Anti-Aging Tablets because they bear drug claims without an approved NDA or ANDA.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically involves a temporary or medically reversible adverse health consequence. The hazard is regulatory (unapproved drug claims) rather than a specific physical injury or contamination, fitting the Moderate criteria for labeling/regulatory issues without reported injuries.
Plain-English summary
Murray International Trading Co., Inc. is recalling 204 bottles of ChingChunBao ANTI-AGING TABLETS. The product is packaged in 80-count bottles within a box with UPC 0 49987 01144 9, and the remaining labeling contains Chinese characters. The recall covers all lots.
The recall was initiated because the product is marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). Although marketed as a dietary supplement, the labeling bears drug or disease claims, which makes the product an unapproved drug under FDA regulations.
The product was distributed nationwide and in Puerto Rico. Consumers who possess this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- ChingChunBao ANTI-AGING TABLETS, packaged in 80-count bottles within a box, UPC 0 49987 01144 9, remaining labeling contains Chinese characters.
- Manufacturer
- Murray International Trading Co., Inc.
- Category
- Drug — Dietary Supplement
- Affected units
- 204
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All lots
Distribution
Part of a larger recall action
This product is one of 14 recalled by Murray International Trading Co., Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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