Class II · Moderate risk
Maximum Strength No Drip Nasal Spray
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
National Drug Code
Is NDC 30142-0388-10 recalled?
nasal · 1 BOTTLE, PUMP in 1 CARTON (30142-388-10) / 30 mL in 1 BOTTLE, PUMP
Yes — this exact package was recalled
3 FDA recalls name the code 30142-0388-10 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
- Oxymetazoline HCl
- Strength
- OXYMETAZOLINE HYDROCHLORIDE .05 g/100mL
- Form
- Spray, Metered · Nasal
- Labeler
- Kroger Company
- Type
- Human OTC Drug
- Product code
- 30142-0388
Recalls naming this package
Class II · Moderate risk
Maximum Strength No Drip Nasal Spray
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Class II · Moderate risk
Nasal Spray Decongestant
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
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
- 30142-0600 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
- 30142-0899 Magnesium Citrate 2
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