Sun Killing Grapefruit
FDA Label NDC 69663-1001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sa Cosmetic for the product Sun Killing Grapefruit (NDC 69663-1001). 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

Otc - Active Ingredient

glycerine


Inactive Ingredient

water, alcohol, butylene glycol, betain, carbomer, adenosine, beta glucan, etc


Otc - Purpose

skin protectant

skin soothing

Otc - Keep Out Of Reach Of Children

keep out of reach of the children

Indications & Usage

use as primary pack for moisturizing relief by applying on skin after using ampoule or serum
gently massage for absorption


Warnings

・Stop using the product when you have skin problems or the product disagrees with your skin
・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
・Don't place the product in any place where it will be subjected to extremely high or low temperatures or direct sunlight.


Dosage & Administration

for external use only

* Please review the disclaimer below.