dentalux anti-cavity fluoride
Generic: sodium monofluorophosphate
Labeler: lidl us, llcDrug Facts
Product Profile
Brand Name
dentalux anti-cavity fluoride
Generic Name
sodium monofluorophosphate
Labeler
lidl us, llc
Dosage Form
PASTE, DENTIFRICE
Routes
Active Ingredients
sodium monofluorophosphate .13 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
71141-186
Product ID
71141-186_77de6540-40df-4421-9242-a418ba5c2074
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2024-06-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71141186
Hyphenated Format
71141-186
Supplemental Identifiers
RxCUI
UPC
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
dentalux anti-cavity fluoride (source: ndc)
Generic Name
sodium monofluorophosphate (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .13 g/100g
Packaging
- 1 TUBE in 1 BOX (71141-186-10) / 113 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "77de6540-40df-4421-9242-a418ba5c2074", "openfda": {"upc": ["4056489867678"], "unii": ["C810JCZ56Q"], "rxcui": ["545626"], "spl_set_id": ["ccf54743-81c2-43f8-9c5c-d4baa85fc18d"], "manufacturer_name": ["Lidl US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (71141-186-10) / 113 g in 1 TUBE", "package_ndc": "71141-186-10", "marketing_start_date": "20240630"}], "brand_name": "dentalux ANTI-CAVITY FLUORIDE", "product_id": "71141-186_77de6540-40df-4421-9242-a418ba5c2074", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "71141-186", "generic_name": "Sodium Monofluorophosphate", "labeler_name": "Lidl US, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dentalux ANTI-CAVITY FLUORIDE", "active_ingredients": [{"name": "SODIUM MONOFLUOROPHOSPHATE", "strength": ".13 g/100g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240630", "listing_expiration_date": "20261231"}