Life Extension Shade Factor SPF30 Lotion

Manufacturer
Quality Supplements and Vitamins, Inc. | Pure Source, LLC
Effective date
2017-01-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:20:35

Label at a glance#

ProductLife Extension Shade Factor SPF30
Active ingredientTITANIUM DIOXIDE
Label structure8 sections

Indications and uses

helps prevent sunburn   if used as directed with other sun protection  measures (see Directions ), descreases the risk of skin cancer and early skin  aging caused by the sun

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 6%, Zinc Oxide 6%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

helps prevent sunburn  

  • if used as directed with other sun protection  measures (see Directions), descreases the risk of skin cancer and early skin  aging caused by the sun

Warnings

WARNINGS SECTION

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

OTC - STOP USE SECTION

if 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
  • Sun Protection Measures. Spending time in the sun increases your risk of skin .cancer and early skin aging. To decrease this risk, regularly use asunscreen with .a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m.to 2 p.m. 
  • wear long-sleeve shirts, pants, hats, and sunglasses
  • children under 6 months of age: Ask a doctor

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe juice, carrot seed extract, chamoile extract, cocoa seed butter, coconut oil, corn propanediol, cucumber fruit extract, green tea leaf extract, gluconolactone, glycerin, licorice root extract, milk thistle fruit extract, niacinamide, oat betaglucan, octyl palmitate, orange oil, rosemary extract, sodium benzoate, sodium hydroxypropylsulfonate laurylglucosides, sunflower seed oil, sweet almond oil, tocopherol (vitamin E), water, watermelon fruit extract, xanthan gum.

Questions or comments?

OTC - QUESTIONS SECTION

1-866-280-2852

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71197-77971197-779-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
074169c3-d0ab-5efe-e063-6294a90a9f5c4675f287-6147-11f0-e054-00144ff88e882023-10-08WarningsExact identifier
spl set id: 4675f287-6147-11f0-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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