Otc - Active Ingredient
ACTIVE INGREDIENTS: OCTINOXATE 7.5%, OCTISALATE 3.5%, TITANIUM DIOXIDE, 1.2%
Youth Surge
FDA Label NDC 49527-730
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Clinique Laboratories Inc for the product Youth Surge (NDC 49527-730). 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 otc - active ingredient, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
WARNING: KEEP OUT OF EYES. STOP USE IF IRRITATION OCCURS. KEEP OUT OF REACH OF CHILDREN.
Package Label.Principal Display Panel
PRINCIPLE DISPLAY PANEL 1.7 OZ CARTON
CLINIQUE
YOUTH SURGE SPF 15
AGE DECELERATING MOISTURIZER
DRY COMBINATION
NET WT. 1.7 OZ/ 50 ML
CLINIQUE LABORATORIES DISTR.
NEW YORK, NY 10022
6NFC
CLINIQUE.COM
Folding Carton (6nfccarton Page 1)
* Please review the disclaimer below.
