Drugplain

Clear System Brightening Day Cream SPF 15 2 g/100mL

OCTOCRYLENE, OCTISALATE · CREAM · Bentley Laboratories, LLC

No Recall History
Plain English

Clear System Brightening Day Cream SPF 15 is a cream containing octocrylene, octisalate at 2 g/100mL, taken topical. Manufactured by Bentley Laboratories, LLC.

Key Facts

Brand Name
Clear System Brightening Day Cream SPF 15
Generic Name
OCTOCRYLENE, OCTISALATE
NDC Code (Product)
54111-187
Manufacturer
Bentley Laboratories, LLC
Strength
2 g/100mL
Dosage Form
CREAM
Route
TOPICAL
Marketing Status
Application #
M020
Marketing Start
12/01/2024

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses •Helps prevent sunburn • if used as directed with other sun protection measures (see Directions ) decreases the risk of skin cancer and early signs of aging from the sun.

Dosage & Administration

Directions • ​ ​ Use in the morning. • Rub cream gently into your entire face and neck, avoiding the eyes.

Warnings

Warnings • For external use only. • Do not use on damaged or broken skin. • When using this product keep out of eyes. Rinse with water to remove. • Stop use and ask doctor if rash occurs.

Frequently Asked Questions

What is Clear System Brightening Day Cream SPF 15 used for?

Clear System Brightening Day Cream SPF 15 contains OCTOCRYLENE, OCTISALATE. It is a cream taken topical. Consult your doctor for specific uses.

Is Clear System Brightening Day Cream SPF 15 a controlled substance?

Clear System Brightening Day Cream SPF 15 is not classified as a controlled substance by the DEA.

What is the generic name for Clear System Brightening Day Cream SPF 15?

The generic name for Clear System Brightening Day Cream SPF 15 is OCTOCRYLENE, OCTISALATE. There are 12 other brand versions of OCTOCRYLENE, OCTISALATE.

What is the NDC code for Clear System Brightening Day Cream SPF 15 2 g/100mL?

The NDC (National Drug Code) for Clear System Brightening Day Cream SPF 15 2 g/100mL is 54111-187, listed by Bentley Laboratories, LLC.