Package 61578-215-01

Brand: pro gel 5000 mint

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 61578-215-01
Digits Only 6157821501
Product NDC 61578-215
Product ID 61578-215_424ae751-1f8e-4e67-ba2e-b368d447053e
Description

68 g in 1 TUBE, WITH APPLICATOR (61578-215-01)

Marketing

Marketing Status
Marketed Since 2022-05-10
Brand pro gel 5000 mint
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

PRO Gel 5000 Mint, PRO Gel 5000 Citrus ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "424ae751-1f8e-4e67-ba2e-b368d447053e", "openfda": {"upc": ["0361578216010", "0361578215013"], "unii": ["8ZYQ1474W7"], "rxcui": ["392038"], "spl_set_id": ["f127e236-5207-948b-e053-2a95a90ab740"], "manufacturer_name": ["DENTAL ALLIANCE HOLDINGS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "68 g in 1 TUBE, WITH APPLICATOR (61578-215-01)", "package_ndc": "61578-215-01", "marketing_start_date": "20220510"}], "brand_name": "PRO Gel 5000 Mint", "product_id": "61578-215_424ae751-1f8e-4e67-ba2e-b368d447053e", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "61578-215", "generic_name": "Sodium fluoride", "labeler_name": "DENTAL ALLIANCE HOLDINGS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRO Gel 5000", "brand_name_suffix": "Mint", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "5000 ug/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20220510", "listing_expiration_date": "20261231"}