Package 0135-0568-04

Brand: sensodyne pronamel multi action

Generic: potassium nitrate and sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 0135-0568-04
Digits Only 0135056804
Product NDC 0135-0568
Product ID 0135-0568_0fb8d5cd-17d5-f0ac-e063-6394a90ab28d
Description

1 TUBE in 1 CARTON (0135-0568-04) / 113 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2013-12-09
Brand sensodyne pronamel multi action
Generic potassium nitrate and sodium fluoride
Sample Package No

Linked Drug Pages (1)

SENSODYNE PRONAMEL Daily Protection, SENSODYNE PRONAMEL Gentle Whitening, SENSODYNE PRONAMEL Fresh Breath, SENSODYNE PRONAMEL Multi Action ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0fb8d5cd-17d5-f0ac-e063-6394a90ab28d", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["edffce4d-108b-4ffd-9adf-e12cb42ffddd"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0135-0568-04)  / 113 g in 1 TUBE", "package_ndc": "0135-0568-04", "marketing_start_date": "20131209"}], "brand_name": "SENSODYNE PRONAMEL Multi Action", "product_id": "0135-0568_0fb8d5cd-17d5-f0ac-e063-6394a90ab28d", "dosage_form": "PASTE", "product_ndc": "0135-0568", "generic_name": "potassium nitrate and sodium fluoride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SENSODYNE PRONAMEL", "brand_name_suffix": "Multi Action", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.15 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20131209", "listing_expiration_date": "20261231"}