Class II · Moderate risk
MenoPower
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
National Drug Code
Is NDC 61096-1014 recalled?
MenoPower
This product was recalled — in other package sizes
No FDA recall names your exact package code, but 1 recall cover the same product (61096-1014) in a different bottle or carton size. Worth checking with your pharmacist.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls of this product
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 61096-0001 See recall 1
- 61096-0002 See recall 1
- 61096-0003 See recall 1
- 61096-0004 See recall 1
- 61096-0005 See recall 1
- 61096-0006 See recall 1
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