anticavity fluoride rinse
Generic: sodium fluoride
Labeler: lidl us, llcDrug Facts
Product Profile
Brand Name
anticavity fluoride rinse
Generic Name
sodium fluoride
Labeler
lidl us, llc
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71141-159
Product ID
71141-159_4a052a47-2017-3a0f-e063-6294a90aaf54
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2017-02-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71141159
Hyphenated Format
71141-159
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
anticavity fluoride rinse (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/mL
Packaging
- 1000 mL in 1 PACKAGE (71141-159-32)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a052a47-2017-3a0f-e063-6294a90aaf54", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["c47475aa-3125-410f-aa31-0add6e4ce125"], "manufacturer_name": ["Lidl US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 PACKAGE (71141-159-32)", "package_ndc": "71141-159-32", "marketing_start_date": "20170209"}], "brand_name": "Anticavity Fluoride Rinse", "product_id": "71141-159_4a052a47-2017-3a0f-e063-6294a90aaf54", "dosage_form": "MOUTHWASH", "product_ndc": "71141-159", "generic_name": "Sodium Fluoride", "labeler_name": "Lidl US, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity Fluoride Rinse", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170209", "listing_expiration_date": "20271231"}