NDC 0135-0181 – Tums Ultra

Calcium Carbonate 1000 mg/1 · Tablet, Chewable · Oral

Human Otc Drug 5 recalls

Product NDC0135-0181

Product details

Brand name
Tums Ultra
Generic name
Calcium carbonate
Labeler
Haleon US Holdings LLC
Dosage form
Tablet, Chewable
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M001
Marketed since
February 12, 2010
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Tums →

Package NDC codes (7)

Package NDCDescriptionSince
0135-0181-013 PACKAGE in 1 CARTON (0135-0181-01) / 12 TABLET, CHEWABLE in 1 PACKAGEFeb 12, 2010
0135-0181-0272 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-02)Feb 12, 2010
0135-0181-0312 TABLET, CHEWABLE in 1 PACKAGE (0135-0181-03)Feb 12, 2010
0135-0181-05265 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-05)Feb 12, 2010
0135-0181-0686 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-06)Feb 12, 2010
0135-0181-071 PACKAGE in 1 CARTON (0135-0181-07) / 12 TABLET, CHEWABLE in 1 PACKAGEFeb 12, 2010
0135-0181-14160 TABLET, CHEWABLE in 1 BOTTLE (0135-0181-14)Feb 12, 2010

Recalls mentioning this NDC

Other Tums products