Class III · Low risk
Colostat
Labeling mix-up - Indications on product label are incorrect.
National Drug Code
Is NDC 44911-0411-01 recalled?
Colostat · 30 mL in 1 BOTTLE, DROPPER (44911-0411-1)
Yes — this exact package was recalled
1 FDA recall names the code 44911-0411-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Rhamnus Purshiana, Spigelia Anthelmia, Taraxacum Officinale, Cajuputum, Hydrastis Canadensis, Alumina, Cina, Cinchona Officinalis, Lycopodium Clavatum, Magnesia Phosphorica, Mandragora Officinarum, Nux Vomica
- Strength
- FRANGULA PURSHIANA BARK 3 [hp_X]/mL; SPIGELIA ANTHELMIA…
- Form
- Liquid · Oral
- Labeler
- Energique, Inc.
- Type
- Human OTC Drug
- Product code
- 44911-0411
Recalls naming this package
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
- 44911-0132 See recall 1
- 44911-0133 See recall 1
- 44911-0134 See recall 1
- 44911-0135 See recall 1
- 44911-0136 See recall 1
- 44911-0137 See recall 1
Free recall alerts
Know the day your medication is recalled
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