Active Ingredient
Homosalate (6.9%), Octinoxate (4.7%), Octisalate (4.0%), Octocrylene (3.4%), Zinc Oxide (5.0%)
Zinka Spf 50 Facestick
FDA Label NDC 52993-150
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zinka for the product Zinka Spf 50 Facestick (NDC 52993-150). 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, purpose, keep out of reach of children, uses, warnings, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Sunscreen
Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control Center right away.
Uses
Helps prevent sunburn.
Warnings
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early aging.
For external use only: Stop use and ask a doctor: if rash or irritation develops and lasts. Keep out of eyes. Rinse with water to remove.
Directions
Apply liberally 15 minutes before sun exposure. Reapply: After 80 minutes of swimming or sweating. Immediately after towel drying. At least every 2 hours.
Inactive Ingredients
BHT, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Cetyl Alcohol, Flavor Methylparaben, Microcrystalline Wax, Ozokerite, Polyethylene, Propylparaben, PVP/Hexadecene Copolymer, Synthetic Beeswax, Tapioca Starch Polymethylsilsesquioxane, Tocopherol,.
* Please review the disclaimer below.
