Walgreens Sunscreen
FDA Label NDC 0363-4014

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Co. for the product Walgreens Sunscreen (NDC 0363-4014). 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, when using this product, questions or comments?:, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Octocrylene    4.0%

Zinc Oxide      5.0%

Purpose

Sunscreen

Uses

  • helps prevent sunburn

Warnings

For external use only.

When Using This Product

Keep out of eyes. Rinse with water to remove.

Questions Or Comments?:

1-800 WALGREENS (1-800-925-4733)


Directions

  • Apply generously before sun exposure
  • Reapply frequently

Inactive Ingredients

Water, Ethylhexyl Stearate, Diisopropyl Adipate, Cetyl Dimethicone, Polyglyceryl-4 Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Beeswax, Isohexadecane, Sodium Chloride, Hydrogenated Castor Oil, Silica, Triethoxycaprylylsilane, Dimethicone,Tocopherol, Disodium EDTA, Aloe Barbadensis Leaf Juice Powder, Sodium Ascorbyl Phosphate, Phenoxyethanol, Methylparaben, Propylparaben.

Principal Display Panel

Well at

Walgreen

SUNSCREEN

Clear Zinc

Broad Spectrum SPF 50

With Zinc Oxide

UVA/UVB Protection

NET WT 1 OZ (28 g)

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