Organic Sunscreen
FDA Label NDC 71371-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nature's Natural Products, Inc for the product Organic Sunscreen (NDC 71371-001). 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 actives, inactives, purpose, directions, warnings, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Actives

Non-Nano Zinc Oxide 20 % 

Inactives

Spring water, Grapeseed oil, Aloe vera, Vegtable wax,Beeswax, Vitamin E, Lecithin, aspen tree bark, fermented horseradish root

Purpose

Helps prevent sunburn if used as directed

Directions

Sun Protection Measures:Spending time in the sun increases your risk of skin cancer and early skin aging
To decrease this risk, regularly use a sunscreen with Broad Spectrum SPF value of 15 or higher and other sun protection measures including:  


 - Limit time in the sun, especially from 10am-2pm    

-  For children under 6 months of age: ask a doctor

 - Wear long-sleeved shirts, pants, hats, and sunglasses                                                  

Warnings

For external use only.
Do not use on skin that is broken or infl­amed if you are allergic to ingredients in this product
When using this product avoid contact with eyes if product gets into eyes, rinse thoroughly with water
Stop use and ask a doctor if rash appears, condition worsens or does not improve in 2-4 weeks
If pregnant or breast-feeding, ask a doctor before use.

Keep out of the reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Product Label

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