Class I ยท High risk
Healthy Living Acetaminophen
Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.
National Drug Code
Is NDC 58602-0882-21 recalled?
Acetaminophen Aspirin and Caffeine · 1 BOTTLE in 1 CARTON (58602-882-21) / 100 TABLET, FILM COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 58602-0882-21 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.
1 of these recalls is still ongoing.
- Active ingredient
- acetaminophen, aspirin and caffeine
- Strength
- ACETAMINOPHEN 250 mg/1; ASPIRIN 250 mg/1; CAFFEINE 65 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Aurohealth LLC
- Type
- Human OTC Drug
- Product code
- 58602-0882
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
- 58602-0711 See recall 1
- 58602-0820 See recall 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.