Active Ingredient
Zinc Oxide 15% (w/w)
Feibth Tallow Sunscreen Cream
FDA Label NDC 85817-002
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 Qiexiran Cosmetics Co., Ltd. for the product Feibth Tallow Sunscreen (NDC 85817-002). 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, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Sunscreen
Use
· Helps prevent sunburn
· 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.
Do Not Use
· on damaged or broken skin
When Using
· keep out of eyes. Rinse with water to remove.
Stop Use
· rash occurs
Ask Doctor
· rash occurs
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a poison control center right away.
Directions
·Apply liberally 15 minutes before sun exposure
·Reapply:
1.After 80 minutes of swimming or sweating
2.Immediately after towel drying
3.At least every 2 hours
Other Information
· Protect this product from excessive heat and direct sun
· May stain some fabrics
Inactive Ingredients
Tallow, Beeswax, Red Raspberry Seed Oil, Carrot Seed Oil, Coconut Oil, Jojoba Oil, Shea Butter
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