anticavity rinse
Generic: sodium fluoride
Labeler: walmart inc.Drug Facts
Product Profile
Brand Name
anticavity rinse
Generic Name
sodium fluoride
Labeler
walmart inc.
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
49035-004
Product ID
49035-004_4bd29ab1-6fdb-5cb4-e063-6294a90a9bdd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2004-04-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49035004
Hyphenated Format
49035-004
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 rinse (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 mg/mL
Packaging
- 532 mL in 1 BOTTLE, PLASTIC (49035-004-44)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bd29ab1-6fdb-5cb4-e063-6294a90a9bdd", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["3beb65e4-ae8e-4e51-b9ba-181cbec41eff"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "532 mL in 1 BOTTLE, PLASTIC (49035-004-44)", "package_ndc": "49035-004-44", "marketing_start_date": "20040406"}], "brand_name": "Anticavity Rinse", "product_id": "49035-004_4bd29ab1-6fdb-5cb4-e063-6294a90a9bdd", "dosage_form": "MOUTHWASH", "product_ndc": "49035-004", "generic_name": "Sodium Fluoride", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity Rinse", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".2 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040406", "listing_expiration_date": "20271231"}