Package 69367-310-56

Brand: sodium fluoride 1.1% gel

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 69367-310-56
Digits Only 6936731056
Product NDC 69367-310
Description

1 TUBE in 1 CARTON (69367-310-56) / 56 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2021-03-09
Brand sodium fluoride 1.1% gel
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "4251b577-cd67-4556-a1cc-207aea831860", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1486566"], "spl_set_id": ["1822c957-0bd6-4e86-a030-80e6e428063a"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69367-310-56)  / 56 g in 1 TUBE", "package_ndc": "69367-310-56", "marketing_start_date": "20210309"}], "brand_name": "Sodium Fluoride 1.1% Gel", "product_id": "69367-310_4251b577-cd67-4556-a1cc-207aea831860", "dosage_form": "GEL", "product_ndc": "69367-310", "generic_name": "Sodium Fluoride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Fluoride 1.1% Gel", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "5 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210309", "listing_expiration_date": "20261231"}