Active Ingredient
ETHYLHEXYL METHOXYCINNAMATE 4％，ETHYLHEXYL SALICYLATE ４％
Melao Tallow Sunscreen Cream
FDA Label NDC 60771-0050
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Haishi Biological Technology Co., Ltd. for the product Melao Tallow Sunscreen (NDC 60771-0050). 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, use, warnings, stop use and ask a doctor if, do not use, when using this product, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Sunscreen
Use
Step1: After using the basic lotion
Step2: Apply appropriate amount to the palm, smear on the whole face, neck and other easily exposed parts
Step3: Apply evenly and gently so that it absorbs into a film
Warnings
For external use only
Stop Use And Ask A Doctor If
rash occurs.
Do Not Use
on damaged or broken skin.
When Using This Product
keep out of eyes. Rinse with water to remove.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage
Squeeze out an appropriate amount of sunscreen and spread evenly on skin.
Inactive Ingredients
WATER，PROPYLENE GLYCOL，GLYCERIN，ALLANTOIN，SODIUM HYALURONATE，BISABOLOL，ADEPS BOVIS，TOCOPHERYL ACETATE，DIMETHICONE，CETEARYL GLUCOSIDE，CETETH-21，CETETH-2，CETEARYL ALCOHOL，CARBOMER，TRIETHANOLAMINE，PHENOXYETHANOL，ETHYLHEXYLGLYCERIN，SAURURUS CHINENSIS LEAF/ROOT EXTRACT，TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT，STEPHANIA TETRANDRA EXTRACT
Principal Display Panel
Label. (00)
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