Class II ยท Moderate risk
Pain Reliever
Failed Impurities/Degradation Specifications: firm's investigation due to customer complaints for discoloration found that the product was out of specification for an impurity.
National Drug Code
Is NDC 0363-9947-35 recalled?
Pain Reliever · 1 BOTTLE in 1 CARTON (0363-9947-35) / 225 TABLET in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 0363-9947-35 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
- Acetaminophen
- Strength
- ACETAMINOPHEN 500 mg/1
- Form
- Tablet · Oral
- Labeler
- Walgreen CO.
- Type
- Human OTC Drug
- Product code
- 0363-9947
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
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