Drug Atlas

NDC 0363-0073 – Soothe

Bismuth Subsalicylate 525 mg/30mL · Liquid · Oral

Human Otc Drug 2 recalls

Product NDC0363-0073

Product details

Brand name: Soothe
Generic name: Bismuth subsalicylate
Labeler: Walgreens
Dosage form: Liquid
Route: Oral
Marketing category: OTC MONOGRAPH DRUG · M008
Marketed since: January 31, 2015
Listing expires: December 31, 2026
Pharmacologic class: Bismuth

Active ingredients

Bismuth Subsalicylate 525 mg/30mL

Uses, dosage, side effects and warnings for Soothe →

Package NDC codes (2)

Package NDC	Description	Since
0363-0073-08	237 mL in 1 BOTTLE, PLASTIC (0363-0073-08)	Jan 31, 2015
0363-0073-16	473 mL in 1 BOTTLE, PLASTIC (0363-0073-16)	Jan 31, 2015

Recalls mentioning this NDC

D-0419-2015 Mar 25, 2015 · Class II
Microbial Contamination of Non-Sterile Products: Lots failed microbiological testing at the 12-month time point.
D-311-2013 May 8, 2013 · Class II
Microbial Contamination of Non-Sterile Products: Lot in question had an elevated microbial count outside of specifications and E. Coli contamination.

Other Soothe products

0363-0736 Bismuth Subsalicylate 525 mg/30mL · Liquid · Walgreens
0363-7240 Bismuth Subsalicylate 525 mg/30mL · Liquid · Walgreens
0363-7370 Bismuth Subsalicylate 525 mg/15mL · Liquid · Walgreens
24208-495 Glycerin 6 mg/mL; Propylene Glycol 6 mg/mL · Solution/ Drops · Bausch & Lomb Incorporated
0363-5960 Calcium Carbonate 400 mg/1 · Tablet, Chewable · Walgreen Company