Package 52000-112-01

Brand: universal advanced whitening anti-cavity fluoride

Generic: sodium monofluorophosphate
NDC Package

Package Facts

Identity

Package NDC 52000-112-01
Digits Only 5200011201
Product NDC 52000-112
Product ID 52000-112_e3086345-3da8-4262-9854-15ab1e031e58
Description

181 g in 1 TUBE (52000-112-01)

Marketing

Marketing Status
Marketed Since 2020-05-30
Brand universal advanced whitening anti-cavity fluoride
Generic sodium monofluorophosphate
Sample Package No

Linked Drug Pages (1)

UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "e3086345-3da8-4262-9854-15ab1e031e58", "openfda": {"unii": ["C810JCZ56Q"], "rxcui": ["545626"], "spl_set_id": ["879dfaf0-27c8-41a3-8d01-a1c3eec9edfc"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "181 g in 1 TUBE (52000-112-01)", "package_ndc": "52000-112-01", "marketing_start_date": "20200530"}], "brand_name": "UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE", "product_id": "52000-112_e3086345-3da8-4262-9854-15ab1e031e58", "dosage_form": "PASTE", "product_ndc": "52000-112", "generic_name": "Sodium Monofluorophosphate", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UNIVERSAL 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": "20200530", "listing_expiration_date": "20261231"}