MedPath

Oral-B Minute-Foam Bubble Gum

Package.Label Principal Display Panel

Approved
Approval ID

d9686d21-6b52-4dc7-b690-4ed785ca1885

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 31, 2010

Manufacturers
FDA

Oral-B Laboratories

DUNS: 183102243

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Acidulated Phosphate Fluoride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0041-0345
Product Classification
G
Generic Name
Acidulated Phosphate Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateAugust 31, 2010
FDA Product Classification

INGREDIENTS (1)

Sodium FluorideActive
Quantity: 10 mg in 1 g
Code: 8ZYQ1474W7
Classification: ACTIM

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Oral-B Minute-Foam Bubble Gum - FDA Drug Approval Details