Package 0363-2123-28

Brand: walgreens multi-antibiotic with pain relief cream

Generic: polymyxin b sulfate, neomycin sulfate, pramoxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-2123-28
Digits Only 0363212328
Product NDC 0363-2123
Product ID 0363-2123_cc7521e6-18ba-45d1-8dba-1151da0162e7
Description

1 TUBE in 1 CARTON (0363-2123-28) / 28 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2015-07-15
Brand walgreens multi-antibiotic with pain relief cream
Generic polymyxin b sulfate, neomycin sulfate, pramoxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Walgreens Multi-Antibiotic with Pain Relief Cream ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "cc7521e6-18ba-45d1-8dba-1151da0162e7", "openfda": {"upc": ["0311917179117"], "unii": ["057Y626693", "19371312D4", "88AYB867L5"], "rxcui": ["1359360"], "spl_set_id": ["f4feccc3-ac25-4d8a-9b68-9a24f755524a"], "manufacturer_name": ["Walgreens Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0363-2123-14)  / 14 g in 1 TUBE", "package_ndc": "0363-2123-14", "marketing_start_date": "20150715"}, {"sample": false, "description": "1 TUBE in 1 CARTON (0363-2123-28)  / 28 g in 1 TUBE", "package_ndc": "0363-2123-28", "marketing_start_date": "20150715"}], "brand_name": "Walgreens Multi-Antibiotic with Pain Relief Cream", "product_id": "0363-2123_cc7521e6-18ba-45d1-8dba-1151da0162e7", "dosage_form": "CREAM", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "0363-2123", "generic_name": "Polymyxin B Sulfate, Neomycin Sulfate, Pramoxine Hydrochloride", "labeler_name": "Walgreens Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Walgreens Multi-Antibiotic with Pain Relief Cream", "active_ingredients": [{"name": "NEOMYCIN SULFATE", "strength": "3.5 mg/g"}, {"name": "POLYMYXIN B SULFATE", "strength": "10000 [USP'U]/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150715", "listing_expiration_date": "20261231"}