anticavity

Generic: sodium fluoride

Labeler: walmart inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name anticavity
Generic Name sodium fluoride
Labeler walmart inc.
Dosage Form MOUTHWASH
Routes
ORAL
Active Ingredients

sodium fluoride .2 mg/mL

Manufacturer
Walmart Inc.

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
313029
UNII
8ZYQ1474W7

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/mL
source: ndc
Packaging
  • 1000 mL in 1 BOTTLE, PLASTIC (49035-581-86)
source: ndc

Packages (1)

Ingredients (1)

sodium fluoride (.2 mg/mL)

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"}