anticavity
Generic: sodium fluoride
Labeler: walmart inc.Drug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
walmart inc.
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
49035-581
Product ID
49035-581_4bd50069-b71a-f46e-e063-6294a90a93f9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2016-09-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49035581
Hyphenated Format
49035-581
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 (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 mg/mL
Packaging
- 1000 mL in 1 BOTTLE, PLASTIC (49035-581-86)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bd50069-b71a-f46e-e063-6294a90a93f9", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["af5b93e7-5cce-4e01-8df2-54494d8b2910"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (49035-581-86)", "package_ndc": "49035-581-86", "marketing_start_date": "20160925"}], "brand_name": "Anticavity", "product_id": "49035-581_4bd50069-b71a-f46e-e063-6294a90a93f9", "dosage_form": "MOUTHWASH", "product_ndc": "49035-581", "generic_name": "Sodium fluoride", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".2 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160925", "listing_expiration_date": "20271231"}