Time Cap Labs recalls 600mg Ibuprofen tablets with 800mg tablets
Time Cap Labs recalls 500-count 600mg Ibuprofen tablets (Rx only) that contain some 800mg tablets. Consumers should check product details and contact the company for guidance.
Lower-risk recall
Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles were found to contain some Ibuprofen Tablets USP 800 mg.
Contact the company
What happened, in plain English
Time Cap Labs is recalling 500-count bottles of 600mg Ibuprofen tablets (Rx only) because some tablets in the bottles are actually 800mg. This could lead to incorrect dosing if taken without knowing the actual strength. Read more at govinfonow.com/recall/41554-time-cap-labs-recalls-600mg-ibuprofen-tablets-with-800mg-tablets.
Source Summary by GovInfoNow · govinfonow.com/recall/41554-time-cap-labs-recalls-600mg-ibuprofen-tablets-with-800mg-tablets · Updated October 8, 2026 · FDA enforcement record: FDA #D-1055-2017
Cite this page
“Time Cap Labs recalls 600mg Ibuprofen tablets with 800mg tablets.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41554-time-cap-labs-recalls-600mg-ibuprofen-tablets-with-800mg-tablets. Based on FDA recall #D-1055-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1055-2017%22&limit=1).
Why it’s dangerous
The recalled tablets contain some 800mg tablets instead of the labeled 600mg. This could cause incorrect dosing if taken without knowing the actual strength, potentially leading to overdose.
Who’s affected
People who have the 500-count 600mg Ibuprofen tablets (Rx only) from Time Cap Labs. Those who take the tablets without checking the actual strength may risk incorrect dosing.
How to tell if you have this one
Check for the 500-count bottle labeled 'Ibuprofen Tablets, USP 600 mg, Capsule Shaped' (Rx only). The product was manufactured by Marksans Pharma Ltd. in India and sold in the US with NDC 49483-603-50.
- Brand
Time Cap Labs- Category
Drug
What to do — step by step
Check Product Details
Look for the 500-count bottle labeled 'Ibuprofen Tablets, USP 600 mg, Capsule Shaped' (Rx only) with NDC 49483-603-50.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide U.S.A.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1055-2017 (June 16, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1055-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.