Active Ingredient
Octinoxate 7.5%
Titanium Dioxide 25%
Oxybenzone 6%
Pro Laser
FDA Label NDC 42248-130
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zenith Medicosm Sl for the product Pro Laser (NDC 42248-130). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, description, warning, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Description
PRO LASER BODY EMULSION
SPF 35
Protective body cream formulated with the perfect combination of sunscreens capable of covering a larger area of the solar radiation spectrum. Indicated for use after laser body treatments and surgery, and for skin that has been subjected to aggressive treatments and that needs extreme protection and rapid regeneration
Apply by rubbing into the skin until completely absorbed. Repeat 2 to 3 times a day. Not water resistant.
150ml. 5.1 fl. Oz
Warning
TOPICAL USE
* Please review the disclaimer below.
