oral antivavity
Generic: sodium fluoride
Labeler: harris teeterDrug Facts
Product Profile
Brand Name
oral antivavity
Generic Name
sodium fluoride
Labeler
harris teeter
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72036-576
Product ID
72036-576_4a045e8b-81d3-5698-e063-6394a90af0d9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2015-01-08
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72036576
Hyphenated Format
72036-576
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
oral antivavity (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 BOTTLE, PLASTIC (72036-576-86)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a045e8b-81d3-5698-e063-6394a90af0d9", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["571f7628-fd59-462f-96dd-67aeaa98cff1"], "manufacturer_name": ["HARRIS TEETER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (72036-576-86)", "package_ndc": "72036-576-86", "marketing_start_date": "20150108"}], "brand_name": "Oral Antivavity", "product_id": "72036-576_4a045e8b-81d3-5698-e063-6394a90af0d9", "dosage_form": "MOUTHWASH", "product_ndc": "72036-576", "generic_name": "Sodium fluoride", "labeler_name": "HARRIS TEETER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Oral Antivavity", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150108", "listing_expiration_date": "20271231"}