Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 12660-0048 recalled?

Tetrahydrozoline Hydrochloride

This product was recalled — in other package sizes

No FDA recall names your exact package code, but 1 recall cover the same product (12660-0048) in a different bottle or carton size. Worth checking with your pharmacist.

Active ingredient
Tetrahydrozoline Hydrochloride
Strength
TETRAHYDROZOLINE HYDROCHLORIDE 1 kg/kg
Form
Powder
Labeler
Societa Italiana Medicinali Scandicci S.I.M.S., SrL
Type
Bulk Ingredient
Product code
12660-0048

Recalls of this product

Class II · Moderate risk

Tetrahydrozoline HCL

CGMP Deviations; Stored/dispensed in a non-GMP compliant warehouse at S.I.M.S., Italy.

Terminated cGMP deviation SST Corporation D-1517-2014

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