Package 81740-003-03

Brand: auraglow whitening

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 81740-003-03
Digits Only 8174000303
Product NDC 81740-003
Product ID 81740-003_3f72b20e-32ad-468c-a67b-ff438c3a8396
Description

1 TUBE in 1 CARTON (81740-003-03) / 113 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-10-20
Brand auraglow whitening
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

Auraglow Whitening ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "3f72b20e-32ad-468c-a67b-ff438c3a8396", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1489127"], "spl_set_id": ["9d45e436-92f6-4a9e-9b82-329847dca9ba"], "manufacturer_name": ["Auraglow LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (81740-003-03)  / 113 g in 1 TUBE", "package_ndc": "81740-003-03", "marketing_start_date": "20251020"}], "brand_name": "Auraglow Whitening", "product_id": "81740-003_3f72b20e-32ad-468c-a67b-ff438c3a8396", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "81740-003", "generic_name": "SODIUM FLUORIDE", "labeler_name": "Auraglow LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Auraglow Whitening", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "2.3 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251020", "listing_expiration_date": "20261231"}