colgate sensitive whitening

Generic: potassium nitrate and sodium fluoride

Labeler: colgate-palmolive company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name colgate sensitive whitening
Generic Name potassium nitrate and sodium fluoride
Labeler colgate-palmolive company
Dosage Form GEL, DENTIFRICE
Routes
DENTAL
Active Ingredients

potassium nitrate 50 mg/g, sodium fluoride 1.1 mg/g

Manufacturer
Colgate-Palmolive Company

Identifiers & Regulatory

Product NDC 35000-131
Product ID 35000-131_12dc4fbb-69dc-449f-ba17-7c2f3723e726
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2027-12-31
Marketing Start 2026-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 35000131
Hyphenated Format 35000-131

Supplemental Identifiers

RxCUI
1038929
UNII
RU45X2JN0Z 8ZYQ1474W7

Packaging Origin

Original Packager
true

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 sensitive whitening (source: ndc)
Generic Name potassium nitrate and sodium fluoride (source: ndc)
Application Number M022 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/g
  • 1.1 mg/g
source: ndc
Packaging
  • 2 TUBE in 1 CARTON (35000-131-34) / 170 g in 1 TUBE
  • 1 TUBE in 1 CARTON (35000-131-46) / 130 g in 1 TUBE
  • 1 TUBE in 1 CARTON (35000-131-60) / 170 g in 1 TUBE
source: ndc

Packages (3)

Ingredients (2)

potassium nitrate (50 mg/g) sodium fluoride (1.1 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "12dc4fbb-69dc-449f-ba17-7c2f3723e726", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1038929"], "spl_set_id": ["3b656928-af58-4ee9-8fb8-360688eb9bf3"], "manufacturer_name": ["Colgate-Palmolive Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TUBE in 1 CARTON (35000-131-34)  / 170 g in 1 TUBE", "package_ndc": "35000-131-34", "marketing_start_date": "20260101"}, {"sample": false, "description": "1 TUBE in 1 CARTON (35000-131-46)  / 130 g in 1 TUBE", "package_ndc": "35000-131-46", "marketing_start_date": "20260101"}, {"sample": false, "description": "1 TUBE in 1 CARTON (35000-131-60)  / 170 g in 1 TUBE", "package_ndc": "35000-131-60", "marketing_start_date": "20260101"}], "brand_name": "Colgate Sensitive Whitening", "product_id": "35000-131_12dc4fbb-69dc-449f-ba17-7c2f3723e726", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "35000-131", "generic_name": "POTASSIUM NITRATE and SODIUM FLUORIDE", "labeler_name": "Colgate-Palmolive Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Colgate Sensitive Whitening", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.1 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260101", "listing_expiration_date": "20271231"}