Ultra Sunscreen .09 g/mL

Octinoxate, Octisalate, Titanium Dioxide · EMULSION · Jiangsu Senwo Medical Technology Co., Ltd.

No Recall History

Plain English

Ultra Sunscreen is a emulsion containing octinoxate, octisalate, titanium dioxide at .09 g/mL, taken topical. Manufactured by Jiangsu Senwo Medical Technology Co., Ltd..

Key Facts

Brand Name: Ultra Sunscreen
Generic Name: Octinoxate, Octisalate, Titanium Dioxide
NDC Code (Product): 85448-003
Manufacturer: Jiangsu Senwo Medical Technology Co., Ltd.
Strength: .09 g/mL
Dosage Form: EMULSION
Route: TOPICAL
Marketing Status
Application #: M020
Marketing Start: 04/07/2026

Recall History

No Recall History

Frequently Asked Questions

What is Ultra Sunscreen used for?

Ultra Sunscreen contains Octinoxate, Octisalate, Titanium Dioxide. It is a emulsion taken topical. Consult your doctor for specific uses.

Is Ultra Sunscreen a controlled substance?

Ultra Sunscreen is not classified as a controlled substance by the DEA.

What is the generic name for Ultra Sunscreen?

The generic name for Ultra Sunscreen is Octinoxate, Octisalate, Titanium Dioxide. There are 11 other brand versions of Octinoxate, Octisalate, Titanium Dioxide.

What is the NDC code for Ultra Sunscreen .09 g/mL?

The NDC (National Drug Code) for Ultra Sunscreen .09 g/mL is 85448-003, listed by Jiangsu Senwo Medical Technology Co., Ltd..

Product NDC

85448-003

Package NDC

85448-003-01

Other Octinoxate, Brands

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)