OTC Medication Information: DAILY LIGHT GUARD DEFENSE FLUID BROAD SPECTRUM SPF 30

DAILY LIGHT GUARD DEFENSE FLUID BROAD SPECTRUM SPF 30- titanium dioxide and zinc oxide lotion
Aveda Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active Ingredients Purpose
Titanium dioxide 6.3% Sunscreen
Zinc oxide 4.1% Sunscreen

Uses

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

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 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

  • shake well. apply generously 15 minutes before sun exposure
  • for sunscreen use, 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 a sunscreen with Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
    • limit time in the sun, especially from 10 a.m.–2 p.m.
    • wear long-sleeve shirts, pants, hats, and sunglasses
  • children under 6 months of age: ask a doctor

Inactive ingredients

Water\Aqua\Eau, Dimethicone, Dicaprylyl Carbonate, Butyloctyl Salicylate, Coco-Caprylate/Caprate, Propanediol, Dipentaerythrityl Tri-Polyhydroxystearate, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Aleurites Moluccana (Kukui) Seed Oil, Trimethylsiloxysilicate, Silica, Hydrogenated Castor Oil/Sebacic Acid Copolymer, Rosmarinus Officinalis (Rosemary) Extract, Helianthus Annuus (Sunflower) Seed Oil, Tocopherol, Caffeine, Punica Granatum (Pomegranate) Extract, Polygonum Cuspidatum, Root Extract, Zingiber Officinale (Ginger) Root Extract, Vanilla Planifolia Fruit Extract, Oryzanol, Ascorbyl Palmitate, Hydroxyapatite, Dimethicone Silylate, Triethoxycaprylylsilane, Dimethicone Crosspolymer-3, Dimethicone/Polyglycerin-3 Crosspolymer, Cetyl PEG/PPG-10/1 Dimethicone, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Caprylyl Glycol, Phenoxyethanol <ILN41846>

Other Information

Protect the product in this container from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL — 30 ml Bottle Carton

AVEDA
THE ART AND SCIENCE OF PURE
FLOWER AND PLANT ESSENCES

daily light
guard

defense fluid
broad spectrum
SPF 30

1 fl oz/oz liq/30 ml e

Principal Display Panel -- 30 ml Bottle Carton
(click image for full-size original)
DAILY LIGHT GUARD DEFENSE FLUID BROAD SPECTRUM SPF 30
titanium dioxide and zinc oxide lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:57677-063
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE 63 mg in 1 mL
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE 41 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
DIMETHICONE
DICAPRYLYL CARBONATE
BUTYLOCTYL SALICYLATE
COCOYL CAPRYLOCAPRATE
PROPANEDIOL
DIPENTAERYTHRITYL TRI-POLYHYDROXYSTEARATE
KUKUI NUT OIL
SILICON DIOXIDE
ROSEMARY
SUNFLOWER OIL
TOCOPHEROL
CAFFEINE
POMEGRANATE
REYNOUTRIA JAPONICA ROOT
GINGER
VANILLA BEAN
ORYZANOL
ASCORBYL PALMITATE
TRIBASIC CALCIUM PHOSPHATE
TRIETHOXYCAPRYLYLSILANE
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE
CAPRYLYL GLYCOL
PHENOXYETHANOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57677-063-01 1 BOTTLE in 1 CARTON contains a BOTTLE
1 30 mL in 1 BOTTLE This package is contained within the CARTON (57677-063-01)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final M020 05/01/2016
Labeler — Aveda Corporation (071352058)
Registrant — Estee Lauder Companies Inc. (790802086)
Establishment
Name Address ID/FEI Operations
The Estee Lauder Inc 802599436 manufacture (57677-063), pack (57677-063), label (57677-063)

Revised: 05/2023 Aveda Corporation

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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