COLGATE OPTIC WHITE RELIEF

Generic: SODIUM FLUORIDE and POTASSIUM NITRATE

Labeler: Colgate-Palmolive Company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Active

Drug Facts

Product Profile

Brand Name COLGATE OPTIC WHITE RELIEF
Generic Name SODIUM FLUORIDE and POTASSIUM NITRATE
Labeler Colgate-Palmolive Company
Dosage Form PASTE, DENTIFRICE
Routes
DENTAL
Active Ingredients

POTASSIUM NITRATE 50 mg/g, SODIUM FLUORIDE 1.5 mg/g

Identifiers & Regulatory

Product NDC 35000-836
Product ID 35000-836_f045e741-2e7c-4f7f-956e-7b4251ba04d1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2025-09-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 35000836
Hyphenated Format 35000-836

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name COLGATE OPTIC WHITE RELIEF (source: ndc)
Generic Name SODIUM FLUORIDE and POTASSIUM NITRATE (source: ndc)
Application Number M021 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/g
  • 1.5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (35000-836-59) / 107 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (2)

POTASSIUM NITRATE (50 mg/g) SODIUM FLUORIDE (1.5 mg/g)

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"}