kaylaan
Generic: zero waste refill for toothpaste
Labeler: kaylaan llcDrug Facts
Product Profile
Brand Name
kaylaan
Generic Name
zero waste refill for toothpaste
Labeler
kaylaan llc
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
sodium fluoride .37 mg/440mg
Manufacturer
Identifiers & Regulatory
Product NDC
82091-116
Product ID
82091-116_2b490a08-149f-76ab-e063-6394a90a084f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Listing Expiration
2026-12-31
Marketing Start
2021-09-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82091116
Hyphenated Format
82091-116
Supplemental Identifiers
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
kaylaan (source: ndc)
Generic Name
zero waste refill for toothpaste (source: ndc)
Application Number
M022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .37 mg/440mg
Packaging
- 74.3 mg in 1 BOX, UNIT-DOSE (82091-116-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "2b490a08-149f-76ab-e063-6394a90a084f", "openfda": {"unii": ["8ZYQ1474W7"], "spl_set_id": ["cb7f5f9b-4192-15e6-e053-2995a90a6457"], "manufacturer_name": ["Kaylaan LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "74.3 mg in 1 BOX, UNIT-DOSE (82091-116-01)", "package_ndc": "82091-116-01", "marketing_start_date": "20210913"}], "brand_name": "KAYLAAN", "product_id": "82091-116_2b490a08-149f-76ab-e063-6394a90a084f", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "82091-116", "generic_name": "Zero Waste Refill For Toothpaste", "labeler_name": "Kaylaan LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "KAYLAAN", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".37 mg/440mg"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210913", "listing_expiration_date": "20261231"}