MedPath

AV3712501 Mineral Sunscreen SPF 18

Drug Facts

Approved
Approval ID

4678375a-492e-4481-9f0c-253a60852de2

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Mar 23, 2011

Manufacturers
FDA

The Hain Celestial Group, Inc.

DUNS: 858894996

Products 1

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

Titanium Dioxide

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code61995-1125
Application Numberpart352
Product Classification
M
Marketing Category
C73604
G
Generic Name
Titanium Dioxide
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 23, 2011
FDA Product Classification

INGREDIENTS (1)

Titanium DioxideActive
Quantity: 7.0 g in 100 g
Code: 15FIX9V2JP
Classification: ACTIB

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