Oral B NeutraCare
Oral B NeutraCare
Approved
Approval ID
8605e7a1-9aa5-476d-8730-1cd663736c73
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 3, 2023
Manufacturers
FDA
YOUNG DENTAL MANUFACTURING CO 1, LLC
DUNS: 006309355
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sodium Fluoride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0273-0241
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 3, 2023
FDA Product Classification
INGREDIENTS (7)
SUCRALOSEInactive
Code: 96K6UQ3ZD4
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
CARBOXYMETHYLCELLULOSE SODIUMInactive
Code: K679OBS311
Classification: IACT
SPEARMINT OILInactive
Code: C3M81465G5
Classification: IACT
PHOSPHORIC ACIDInactive
Code: E4GA8884NN
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
SODIUM FLUORIDEActive
Quantity: 0.5 mg in 1 g
Code: 8ZYQ1474W7
Classification: ACTIM