Package 35000-836-59
Brand: COLGATE OPTIC WHITE RELIEF
Generic: SODIUM FLUORIDE and POTASSIUM NITRATEPackage 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
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"}