2.75% Octinsalate, 7.50% Octinoxate, 8.00% Zinc Oxide Sunscreen

FDA Drug Profile — Private Label Super Light Oil-Free SPF45

Drug Details

Generic Name
2.75% Octinsalate, 7.50% Octinoxate, 8.00% Zinc Oxide Sunscreen
Brand Names
Private Label Super Light Oil-Free SPF45
Application Number
M020
Sponsor
Swiss-American CDMO, LLC
NDC Codes
1
Dosage Forms
LOTION
Routes
TOPICAL
Active Ingredients
OCTINOXATE, OCTISALATE, ZINC OXIDE

Indications and Usage

Use Helps prevent sunburn. If used as directed with other sun protection measures (See directions), decreases the risk of skin cancer and early skin aging caused by the sun.

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 physician if rash occurs. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away