Fruit of the Earth Vitamin E SPF 15 Sunscreen Daily Defense Moisturizer

Manufacturer
FRUIT OF THE EARTH, INC.
Effective date
2024-10-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:51:55

Label at a glance#

ProductFruit of the Earth Vitamin E SPF 15 Sunscreen Daily Defense Moisturizer
Active ingredientOCTINOXATE, OCTOCRYLENE, OXYBENZONE, AVOBENZONE
Label structure12 sections

Indications and uses

helps prevent sunburn

Dosage and administration

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

Storage and handling

protect the product in this container from excessive heat and direct sun may stain or damage some fabrics, materials or surfaces

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.5%, Octisalate 5.0%, Oxybenzone 3.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn

Warnings

WARNINGS SECTION

Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging.

For external use only

Do not use

OTC - DO NOT USE SECTION

• on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

• rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

  • protect the product in this container from excessive heat and direct sun
  • may stain or damage some fabrics, materials or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, aloe barbadensis leaf juice, c12-15 alkyl benzoate, cyclopentasiloxane, phenyl trimethicone, acrylates copolymer, propylene glycol, stearic acid, glyceryl stearate, PEG 100 stearate, tocopheryl acetate (vitamin E), acrylates/steareth-20 methacrylate copolymer, triethanolamine, citrus limon (lemon) fruit oil, methylparaben, propylparaben, ethylparaben, butylparaben, phenoxyethanol, isobutylparaben, disodium EDTA, fragrance, titanium dioxide.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

960E2960E2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62217-25262217-252-33

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
24c7df0f-c5f1-4573-e063-6394a90a6950f5415e74-668a-6038-e053-2995a90a700c2024-10-18WarningsExact identifier
spl id: 24c7df0f-c5f1-4573-e063-6394a90a6950
spl set id: f5415e74-668a-6038-e053-2995a90a700c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.