Active Ingredients
Zinc Oxide 7%
Sojo Sunscreen Lotion
FDA Label NDC 83566-603
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Aimu Biological Technology Co., Ltd for the product Sojo Sunscreen (NDC 83566-603). 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 ingredients, purpose, uses, warnings, stop use, do not use, when using, 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
Uses
helps prevent sunburn.
Warnings
For external use only
Stop Use
and ask a doctor if rash occurs.
Do Not Use
on damaged or broken skin.
When Using
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.
Inactive Ingredients
Water，Propylene Glycol， Glycerin，C12-15 AlkylBenzoate，Phenyl Trimethicone，Trimethylsiloxysilicate，Cetearyl Glucoside ，Cetearyl Alcoho，Glyceryl Stearate，PEG-100 Stearate，OLEA EUROPAEA (OLIVE) FRUIT OIL ，CocosNucifera (Coconut) Oil ，Tocopheryl Acetate，Dipotassium Glycyrrhizate，Sodium Hyaluronate，Carbomer，Triethanolamin，Xanthan Gum，Oryza Sativa (Rice) Extract，Phragmites Communis Extract，Zea Mays (Corn)Silk Extract，Va Sylvestris (Mallow) Flower/Leaf/Stem Extract ，Disodium EDTA，Phenoxyethanol，Ethylhexylglycerin ，StephaniaTetrandra Extract，Taraxacum Officinale LeafExtract，Saururus Chinensis Leaf/Root Extract
Dosage & Administration
Apply liberally 15 minutes before sun exposure.
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