Package 0363-7370-04

Brand: soothe ultra strength

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 0363-7370-04
Digits Only 0363737004
Product NDC 0363-7370
Product ID 0363-7370_931dd60d-ef3f-4395-8bf3-3dd11676a6d0
Description

118 mL in 1 BOTTLE, PLASTIC (0363-7370-04)

Marketing

Marketing Status
Marketed Since 2020-01-31
Brand soothe ultra strength
Generic bismuth subsalicylate
Sample Package No

Linked Drug Pages (1)

Soothe Ultra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "931dd60d-ef3f-4395-8bf3-3dd11676a6d0", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308763"], "spl_set_id": ["ec96e6f2-b087-457e-9b95-30f3595deebb"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, PLASTIC (0363-7370-04)", "package_ndc": "0363-7370-04", "marketing_start_date": "20200131"}], "brand_name": "Soothe Ultra Strength", "product_id": "0363-7370_931dd60d-ef3f-4395-8bf3-3dd11676a6d0", "dosage_form": "LIQUID", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "0363-7370", "generic_name": "Bismuth subsalicylate", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Soothe", "brand_name_suffix": "Ultra Strength", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "525 mg/15mL"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200131", "listing_expiration_date": "20261231"}