Package 52000-108-01

Brand: advanced whitening anti cavity fluoride

Generic: sodium monofluorophosphate
NDC Package

Package Facts

Identity

Package NDC 52000-108-01
Digits Only 5200010801
Product NDC 52000-108
Product ID 52000-108_ede5654c-864e-44c6-904b-ca2ac4532096
Description

181 g in 1 TUBE (52000-108-01)

Marketing

Marketing Status
Marketed Since 2020-05-18
Brand advanced whitening anti cavity fluoride
Generic sodium monofluorophosphate
Sample Package No

Linked Drug Pages (1)

ADVANCED WHITENING ANTI CAVITY FLUORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "ede5654c-864e-44c6-904b-ca2ac4532096", "openfda": {"unii": ["C810JCZ56Q"], "rxcui": ["545626"], "spl_set_id": ["8ea8a8d9-b7e4-468f-9a09-4ec634cbd80e"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "181 g in 1 TUBE (52000-108-01)", "package_ndc": "52000-108-01", "marketing_start_date": "20200518"}], "brand_name": "ADVANCED WHITENING ANTI CAVITY FLUORIDE", "product_id": "52000-108_ede5654c-864e-44c6-904b-ca2ac4532096", "dosage_form": "PASTE", "product_ndc": "52000-108", "generic_name": "Sodium Monofluorophosphate", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ADVANCED WHITENING ANTI CAVITY FLUORIDE", "active_ingredients": [{"name": "SODIUM MONOFLUOROPHOSPHATE", "strength": ".76 g/100g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200518", "listing_expiration_date": "20261231"}