Class III · Low risk
Nicotine polacrilex lozenge
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
National Drug Code
Is NDC 30142-0664-01 recalled?
Antispetic
Yes — this exact package was recalled
1 FDA recall names the code 30142-0664-01 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
- Eucalyptol, menthol, methyl salicylate, thymol
- Strength
- EUCALYPTOL .92 mg/mL; MENTHOL .42 mg/mL; METHYL SALICYLATE…
- Form
- Mouthwash · Oral
- Labeler
- The Kroger Co.
- Type
- Human OTC Drug
- Product code
- 30142-0664
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
- 30142-0388 nasal 3
- 30142-0600 See recall 3
- 30142-0766 infants pain and fever 3
- 30142-0810 70% Isopropyl Rubbing Alcohol 2
- 30142-0818 Childrens Pain and Fever 2
- 30142-0891 See recall 2
Free recall alerts
Know the day your medication is recalled
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