Class II · Moderate risk
Acetaminophen Infant Dye Free Grape Oral Suspension
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
National Drug Code
Is NDC 11673-0133-16 recalled?
up and up acetaminophen infants · 1 BOTTLE in 1 CARTON (11673-133-16) / 59 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 11673-0133-16 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 160 mg/5mL
- Form
- Suspension · Oral
- Labeler
- Target Corporation
- Type
- Human OTC Drug
- Product code
- 11673-0133
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
- 11673-0950 See recall 3
- 11673-0023 See recall 2
- 11673-0876 See recall 2
- 11673-0059 Daytime Cold and Cough and NightTime Cold and Congestion Childrens 1
- 11673-0105 Up and Up childrens acetaminophen 1
- 11673-0130 Up and Up Childrens acetaminophen 1
Free recall alerts
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