MedPath

Oral-B Minute-Foam Strawberry

Package.Label Principal Display Panel

Approved
Approval ID

516801f7-ba4f-4716-bd1f-af4e322675b6

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Sep 2, 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 Code0041-0346
Product Classification
G
Generic Name
Acidulated Phosphate Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateSeptember 2, 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 Strawberry - FDA Drug Approval Details