Otc - Active Ingredient
Ethylhexyl Methoxycinnamate, Zinc Oxide, Ethylhexyl Salicylate, Titanium Dioxide, Octocrylene
Solco Platino Plus Uv Sun
FDA Label NDC 72370-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Solco Biomedical Co., Ltd. for the product Solco Platino Plus Uv Sun (NDC 72370-0001). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Water, Butylene Glycol, Etc
Otc - Purpose
Sunscreen
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Take an appropriate amount of this product and spread evenly on the skin.
Warnings
1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children
Dosage & Administration
for external use only
* Please review the disclaimer below.
