mouth rinse
Generic: sodium fluoride
Labeler: walgreen co.Drug Facts
Product Profile
Brand Name
mouth rinse
Generic Name
sodium fluoride
Labeler
walgreen co.
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0363-0163
Product ID
0363-0163_4aa46dbb-3e7c-cd84-e063-6394a90ad744
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2006-03-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03630163
Hyphenated Format
0363-0163
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
mouth 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 BOTTLE, PLASTIC (0363-0163-86)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4aa46dbb-3e7c-cd84-e063-6394a90ad744", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1038904"], "spl_set_id": ["eae87899-3eba-4d50-bc31-9eaf54ff9e00"], "manufacturer_name": ["Walgreen Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (0363-0163-86)", "package_ndc": "0363-0163-86", "marketing_start_date": "20060315"}], "brand_name": "Mouth Rinse", "product_id": "0363-0163_4aa46dbb-3e7c-cd84-e063-6394a90ad744", "dosage_form": "MOUTHWASH", "product_ndc": "0363-0163", "generic_name": "sodium fluoride", "labeler_name": "Walgreen Co.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mouth Rinse", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20060315", "listing_expiration_date": "20271231"}