Class II · Moderate risk
Infant's Grape Flavored Acetaminophen Oral Suspension
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
National Drug Code
Is NDC 49035-0946-16 recalled?
equate pain and fever infants · 1 BOTTLE in 1 CARTON (49035-946-16) / 59 mL in 1 BOTTLE
Yes — this exact package was recalled
2 FDA recalls name the code 49035-0946-16 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
- Wal-Mart Stores Inc
- Type
- Human OTC Drug
- Product code
- 49035-0946
Recalls naming this package
Class II · Moderate risk
Acetaminophen suspension liquid
Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
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
- 49035-0882 See recall 3
- 49035-0125 See recall 2
- 49035-0229 Acne Treatment 2
- 49035-0273 See recall 2
- 49035-0313 Equate Childrens Pain and Fever 2
- 49035-0404 See recall 2
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