Package 35000-836-59

Brand: COLGATE OPTIC WHITE RELIEF

Generic: SODIUM FLUORIDE and POTASSIUM NITRATE
NDC Package

Package Facts

Identity

Package NDC 35000-836-59
Digits Only 3500083659
Product NDC 35000-836
Description

1 TUBE in 1 CARTON (35000-836-59) / 107 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-09-25
Brand COLGATE OPTIC WHITE RELIEF
Generic SODIUM FLUORIDE and POTASSIUM NITRATE
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "f045e741-2e7c-4f7f-956e-7b4251ba04d1", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1038929"], "spl_set_id": ["c4ce74ba-6b69-4b55-be5d-185f9d9c3c2e"], "manufacturer_name": ["Colgate-Palmolive Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (35000-836-59)  / 107 g in 1 TUBE", "package_ndc": "35000-836-59", "marketing_start_date": "20250925"}], "brand_name": "COLGATE OPTIC WHITE RELIEF", "product_id": "35000-836_f045e741-2e7c-4f7f-956e-7b4251ba04d1", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "35000-836", "generic_name": "SODIUM FLUORIDE and POTASSIUM NITRATE", "labeler_name": "Colgate-Palmolive Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "COLGATE OPTIC WHITE RELIEF", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.5 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250925", "listing_expiration_date": "20261231"}