Drugplain

Softlips Vanilla 20 mg/g

dimethicone, octinoxate, octisalate, oxybenzone · OINTMENT · The Mentholatum Company

No Recall History
Plain English

Softlips Vanilla is a ointment containing dimethicone, octinoxate, octisalate, oxybenzone at 20 mg/g, taken topical. Manufactured by The Mentholatum Company.

Key Facts

Brand Name
Softlips Vanilla
Generic Name
dimethicone, octinoxate, octisalate, oxybenzone
NDC Code (Product)
10742-3051
Manufacturer
The Mentholatum Company
Strength
20 mg/g
Dosage Form
OINTMENT
Route
TOPICAL
Marketing Status
Application #
M020
Marketing Start
11/19/1997

Recall History

No Recall History

Frequently Asked Questions

What is Softlips Vanilla used for?

Softlips Vanilla contains dimethicone, octinoxate, octisalate, oxybenzone. It is a ointment taken topical. Consult your doctor for specific uses.

Is Softlips Vanilla a controlled substance?

Softlips Vanilla is not classified as a controlled substance by the DEA.

What is the generic name for Softlips Vanilla?

The generic name for Softlips Vanilla is dimethicone, octinoxate, octisalate, oxybenzone. There are 11 other brand versions of dimethicone, octinoxate, octisalate, oxybenzone.

What is the NDC code for Softlips Vanilla 20 mg/g?

The NDC (National Drug Code) for Softlips Vanilla 20 mg/g is 10742-3051, listed by The Mentholatum Company.