Class II · Moderate risk
GOODSENSE Ultra Strength
Presence of foreign substance: small metallic particles in chewable tablets.
National Drug Code
Is NDC 50804-0171-68 recalled?
GOODSENSE Ultra Strength Antacid Assorted Fruit · 72 TABLET, CHEWABLE in 1 BOTTLE (50804-171-68)
Yes — this exact package was recalled
1 FDA recall names the code 50804-0171-68 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
- Calcium carbonate
- Strength
- CALCIUM CARBONATE 1000 mg/1
- Form
- Tablet, Chewable · Oral
- Labeler
- GoodSense
- Type
- Human OTC Drug
- Product code
- 50804-0171
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
- 50804-0141 GoodSense Eye Drops Original Formula 2
- 50804-0160 GoodSense Ultra Lubricant Eye Drops 2
- 50804-0110 Good Sense Artificial Tears 1
- 50804-0129 GoodSense Extra Strength Antacid 1
- 50804-0130 GoodSense Eye Drops Advanced Relief Moisturizer 1
- 50804-0164 citroma 1
Free recall alerts
Know the day your medication is recalled
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