Dr. Mercola Broad Spectrum Cream
FDA Label NDC 71239-786

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Natural Health Partners, Llc for the product Dr. Mercola Broad Spectrum (NDC 71239-786). 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, do not use, when using this product, stop use and ask a doctor if, 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

Active Ingredients

Titanium Dioxide (6.0%)

Zinc Oxide (22.5%)

Purpose

Sunscreen

Uses

  • helps prevent sunburn

Warnings

For external use only

Do Not Use

  • on damaged or broken skin

When Using This Product

  • keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor If

  • rash occurs

Keep Out Of Reach Of Children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • apply liberally 15 minutes before sun exposure
  • children under 6 months of age: Ask a doctor
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating

Other Information

  • protect the product in this container from excessive heat and direct sun

Inactive Ingredients

Water (Aqua), Helianthus annuus (Sunflower) Seed Oil, Lecithin, Glycerin, Cocos nucifera (Coconut) Oil, Butyrospermum parkii (Shea) Butter, Camellia sinensis Leaf Extract, Xanthan Gum, Simmondsia chinensis (Jojoba) Seed Oil, Tocopherol, Gluconolactone, Eucalyptus globulus Leaf Oil.

Package Labeling:

Label2 (Label2)

Label2 (Label2)

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