tidalove
Generic: yuzu mint toothpaste tablets
Labeler: paranmare llcDrug Facts
Product Profile
Brand Name
tidalove
Generic Name
yuzu mint toothpaste tablets
Labeler
paranmare llc
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
sodium fluoride .32 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82756-221
Product ID
82756-221_40946943-21d0-b114-e063-6394a90aed3f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2025-10-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82756221
Hyphenated Format
82756-221
Supplemental Identifiers
UPC
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
tidalove (source: ndc)
Generic Name
yuzu mint toothpaste tablets (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .32 mg/1
Packaging
- 62 TABLET, CHEWABLE in 1 POUCH (82756-221-62)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "40946943-21d0-b114-e063-6394a90aed3f", "openfda": {"upc": ["8809130165847"], "unii": ["8ZYQ1474W7"], "spl_set_id": ["40946943-21cf-b114-e063-6394a90aed3f"], "manufacturer_name": ["Paranmare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "62 TABLET, CHEWABLE in 1 POUCH (82756-221-62)", "package_ndc": "82756-221-62", "marketing_start_date": "20251001"}], "brand_name": "Tidalove", "product_id": "82756-221_40946943-21d0-b114-e063-6394a90aed3f", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "82756-221", "generic_name": "Yuzu Mint Toothpaste Tablets", "labeler_name": "Paranmare LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tidalove", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".32 mg/1"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251001", "listing_expiration_date": "20261231"}