Active Ingredients
ETHYLHEXYL METHOXYCINNAMATE
ETHYLHEXYL SALICYLATE
Pure Velocity Tallow Sunscreen Spf 50 Cream
FDA Label NDC 60771-0036
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 Pure Velocity Tallow Sunscreen Spf 50 (NDC 60771-0036). 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
If used as directed with other sun protection measures(see Directions)，
decreases the risk of skin cancer and early skin aging caused by the sun.
Warnings
For external use only
Stop Use
Rinse with wate to remove.
Stop use and ask doctor if rash occurs.
Do Not Use
Do not use on damaged or broken skin.
When Using
When using this product keep out of eyes.
Keep Out Of Reach Of Children
Keep Out Of Reach Of Children
Dosage & Administration
Squeeze out an appropriate amount of Sunscreen and spread evenly on skin.
Inactive Ingredients
WATER
ADEPS BOVIS
PROPYLENE GLYCOL
GLYCERIN
SAURURUS CHINENSIS LEAF/ROOT EXTRACT
CETEARYL ALCOHOL
CETETH-2
TOCOPHERYL ACETATE
DIMETHICONE
CETEARYL GLUCOSIDE
CETETH-21
TARAXACUM OFFICINALE (Dandelion) Leaf Extract
PHENOXYETHANOL
ALLANTOIN
BISABOLOL
CARBOMER
TRIETHANOLAMINE
SODIUM HYALURONATE
ETHYLHEXYLGLYCERIN
STEPHANIA TETRANDRA EXTRACT
Package Label.Principal Display Panel
Label. (00)
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