whitening

Generic: monofluorophosphate

Labeler: target
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name whitening
Generic Name monofluorophosphate
Labeler target
Dosage Form PASTE, DENTIFRICE
Routes
DENTAL
Active Ingredients

sodium monofluorophosphate .14 g/100g

Manufacturer
Target

Identifiers & Regulatory

Product NDC 11673-385
Product ID 11673-385_441eb113-64d9-ceeb-e063-6394a90a2f74
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2024-02-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673385
Hyphenated Format 11673-385

Supplemental Identifiers

RxCUI
545626
UPC
0085239929506
UNII
C810JCZ56Q

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 whitening (source: ndc)
Generic Name monofluorophosphate (source: ndc)
Application Number M021 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • .14 g/100g
source: ndc
Packaging
  • 2 TUBE in 1 CARTON (11673-385-09) / 113 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

sodium monofluorophosphate (.14 g/100g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "441eb113-64d9-ceeb-e063-6394a90a2f74", "openfda": {"upc": ["0085239929506"], "unii": ["C810JCZ56Q"], "rxcui": ["545626"], "spl_set_id": ["0074630f-9d8d-9209-e063-6294a90a4f01"], "manufacturer_name": ["Target"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TUBE in 1 CARTON (11673-385-09)  / 113 g in 1 TUBE", "package_ndc": "11673-385-09", "marketing_start_date": "20250124"}], "brand_name": "Whitening", "product_id": "11673-385_441eb113-64d9-ceeb-e063-6394a90a2f74", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "11673-385", "generic_name": "Monofluorophosphate", "labeler_name": "Target", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Whitening", "active_ingredients": [{"name": "SODIUM MONOFLUOROPHOSPHATE", "strength": ".14 g/100g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240210", "listing_expiration_date": "20261231"}