dentalux anti-cavity fluoride whitening mint
Generic: sodium fluoride
Labeler: lidl us, llcDrug Facts
Product Profile
Brand Name
dentalux anti-cavity fluoride whitening mint
Generic Name
sodium fluoride
Labeler
lidl us, llc
Dosage Form
PASTE, DENTIFRICE
Routes
Active Ingredients
sodium fluoride .243 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
71141-185
Product ID
71141-185_6e4327b9-2172-4b85-a024-f04a166a330d
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
71141185
Hyphenated Format
71141-185
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 whitening mint (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .243 g/100g
Packaging
- 1 TUBE in 1 BOX (71141-185-10) / 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": "6e4327b9-2172-4b85-a024-f04a166a330d", "openfda": {"upc": ["4056489867692"], "unii": ["8ZYQ1474W7"], "rxcui": ["891775"], "spl_set_id": ["37011052-16ef-4ae4-aade-a86f9fa9cdac"], "manufacturer_name": ["Lidl US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (71141-185-10) / 113 g in 1 TUBE", "package_ndc": "71141-185-10", "marketing_start_date": "20240630"}], "brand_name": "dentalux ANTI-CAVITY FLUORIDE WHITENING MINT", "product_id": "71141-185_6e4327b9-2172-4b85-a024-f04a166a330d", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "71141-185", "generic_name": "Sodium Fluoride", "labeler_name": "Lidl US, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dentalux ANTI-CAVITY FLUORIDE WHITENING MINT", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".243 g/100g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240630", "listing_expiration_date": "20261231"}