advance white extreme whitening tartar control

Generic: sodium fluoride

Labeler: church & dwight co., inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name advance white extreme whitening tartar control
Generic Name sodium fluoride
Labeler church & dwight co., inc.
Dosage Form PASTE, DENTIFRICE
Routes
DENTAL
Active Ingredients

sodium fluoride 2.4 mg/g

Manufacturer
Church & Dwight Co., Inc.

Identifiers & Regulatory

Product NDC 10237-658
Product ID 10237-658_44fa11f4-4ddd-e970-e063-6394a90a307e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2012-01-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10237658
Hyphenated Format 10237-658

Supplemental Identifiers

RxCUI
416783
UNII
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 advance white extreme whitening tartar control (source: ndc)
Generic Name sodium fluoride (source: ndc)
Application Number M021 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 2.4 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (10237-658-09) / 25 g in 1 TUBE
  • 2 TUBE in 1 CARTON (10237-658-12) / 340 g in 1 TUBE
  • 2 CARTON in 1 PACKAGE (10237-658-28) / 2 TUBE in 1 CARTON / 204 g in 1 TUBE
  • 1 TUBE in 1 CARTON (10237-658-43) / 121 g in 1 TUBE
  • 4 CARTON in 1 PACKAGE (10237-658-46) / 1 TUBE in 1 CARTON / 170 g in 1 TUBE
  • 1 TUBE in 1 CARTON (10237-658-60) / 170 g in 1 TUBE
source: ndc

Packages (6)

10237-658-09 1 TUBE in 1 CARTON (10237-658-09) / 25 g in 1 TUBE 10237-658-12 2 TUBE in 1 CARTON (10237-658-12) / 340 g in 1 TUBE 10237-658-28 2 CARTON in 1 PACKAGE (10237-658-28) / 2 TUBE in 1 CARTON / 204 g in 1 TUBE 10237-658-43 1 TUBE in 1 CARTON (10237-658-43) / 121 g in 1 TUBE 10237-658-46 4 CARTON in 1 PACKAGE (10237-658-46) / 1 TUBE in 1 CARTON / 170 g in 1 TUBE 10237-658-60 1 TUBE in 1 CARTON (10237-658-60) / 170 g in 1 TUBE

Ingredients (1)

sodium fluoride (2.4 mg/g)

Linked Drug Pages (1)

Advance White Extreme Whitening Tartar Control ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "44fa11f4-4ddd-e970-e063-6394a90a307e", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["416783"], "spl_set_id": ["b539264f-e1ff-440b-af76-84266fe2c0a2"], "manufacturer_name": ["Church & Dwight Co., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (10237-658-09)  / 25 g in 1 TUBE", "package_ndc": "10237-658-09", "marketing_start_date": "20120129"}, {"sample": false, "description": "2 TUBE in 1 CARTON (10237-658-12)  / 340 g in 1 TUBE", "package_ndc": "10237-658-12", "marketing_start_date": "20190923"}, {"sample": false, "description": "2 CARTON in 1 PACKAGE (10237-658-28)  / 2 TUBE in 1 CARTON / 204 g in 1 TUBE", "package_ndc": "10237-658-28", "marketing_start_date": "20240603"}, {"sample": false, "description": "1 TUBE in 1 CARTON (10237-658-43)  / 121 g in 1 TUBE", "package_ndc": "10237-658-43", "marketing_start_date": "20120129"}, {"sample": false, "description": "4 CARTON in 1 PACKAGE (10237-658-46)  / 1 TUBE in 1 CARTON / 170 g in 1 TUBE", "package_ndc": "10237-658-46", "marketing_start_date": "20220426"}, {"sample": false, "description": "1 TUBE in 1 CARTON (10237-658-60)  / 170 g in 1 TUBE", "package_ndc": "10237-658-60", "marketing_start_date": "20120129"}], "brand_name": "Advance White Extreme Whitening Tartar Control", "product_id": "10237-658_44fa11f4-4ddd-e970-e063-6394a90a307e", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "10237-658", "generic_name": "Sodium Fluoride", "labeler_name": "Church & Dwight Co., Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advance White Extreme Whitening", "brand_name_suffix": "Tartar Control", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "2.4 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120129", "listing_expiration_date": "20261231"}