AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE, OCTISALATE

FDA Drug Profile — LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g

AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE, OCTISALATE is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g. Available dosage form: lotion.

Drug Details

Generic Name
AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE, OCTISALATE
Brand Names
LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g
Application Number
M020
Sponsor
DONGDONGGURIMOO CO.,LTD.
NDC Codes
1
Dosage Forms
LOTION
Routes
TOPICAL
Active Ingredients
AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE, OCTISALATE

Indications and Usage

Uses 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