advanced whitening anti cavity fluoride
Generic: sodium monofluorophosphate
Labeler: universal distribution center llcDrug Facts
Product Profile
Brand Name
advanced whitening anti cavity fluoride
Generic Name
sodium monofluorophosphate
Labeler
universal distribution center llc
Dosage Form
PASTE
Routes
Active Ingredients
sodium monofluorophosphate .76 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
52000-108
Product ID
52000-108_ede5654c-864e-44c6-904b-ca2ac4532096
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2020-05-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52000108
Hyphenated Format
52000-108
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
advanced whitening anti cavity fluoride (source: ndc)
Generic Name
sodium monofluorophosphate (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .76 g/100g
Packaging
- 181 g in 1 TUBE (52000-108-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "ede5654c-864e-44c6-904b-ca2ac4532096", "openfda": {"unii": ["C810JCZ56Q"], "rxcui": ["545626"], "spl_set_id": ["8ea8a8d9-b7e4-468f-9a09-4ec634cbd80e"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "181 g in 1 TUBE (52000-108-01)", "package_ndc": "52000-108-01", "marketing_start_date": "20200518"}], "brand_name": "ADVANCED WHITENING ANTI CAVITY FLUORIDE", "product_id": "52000-108_ede5654c-864e-44c6-904b-ca2ac4532096", "dosage_form": "PASTE", "product_ndc": "52000-108", "generic_name": "Sodium Monofluorophosphate", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ADVANCED WHITENING ANTI CAVITY FLUORIDE", "active_ingredients": [{"name": "SODIUM MONOFLUOROPHOSPHATE", "strength": ".76 g/100g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200518", "listing_expiration_date": "20261231"}