Package 0135-0605-01

Brand: aquafresh sensitive maximum strength

Generic: potassium nitrate and sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 0135-0605-01
Digits Only 0135060501
Product NDC 0135-0605
Product ID 0135-0605_0e988328-62da-43e7-98b3-5d94a4cd6684
Description

1 TUBE in 1 CARTON (0135-0605-01) / 158.8 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2017-02-17
Brand aquafresh sensitive maximum strength
Generic potassium nitrate and sodium fluoride
Sample Package No

Linked Drug Pages (1)

AQUAFRESH SENSITIVE MAXIMUM STRENGTH ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "0e988328-62da-43e7-98b3-5d94a4cd6684", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1038929"], "spl_set_id": ["76adbccb-0812-4407-a6fc-a57e6f144fbb"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0135-0605-01)  / 158.8 g in 1 TUBE", "package_ndc": "0135-0605-01", "marketing_start_date": "20170217"}], "brand_name": "AQUAFRESH SENSITIVE MAXIMUM STRENGTH", "product_id": "0135-0605_0e988328-62da-43e7-98b3-5d94a4cd6684", "dosage_form": "PASTE", "product_ndc": "0135-0605", "generic_name": "potassium nitrate and sodium fluoride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AQUAFRESH", "brand_name_suffix": "SENSITIVE MAXIMUM STRENGTH", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.1 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170217", "listing_expiration_date": "20261231"}