Elta MD UV Clear description, usages, side effects, indications, overdosage, supplying and lots more!

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Elta MD UV Clear

Swiss American Products,Inc.
Swiss American Products,Inc.

Elta MD UV Clear SPF46




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients      Purpose

Zinc Oxide 9.0%      Sunscreen

Octinoxate 7.5%      Sunscreen

Uses

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 the product keep out of eyes. Rinse with water to remove
  • Stop use and ask a physician 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 to face and neck 15 minutes before sun exposure
  • use a water-resistant sunscreen if swimming or sweating
  • reapply at least every 2 hours
  • 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 a broad-spectrum SPF 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: Ask a physician

Inactive ingredients

Purified water, Cyclopentasiloxane, Niacinamide, Octyldodecyl Neopentanoate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyisobutene, PEG-7 Trimethylolpropane Coconut Ether, Sodium Hyaluronate, Tocopheryl Acetate, Lactic Acid, Oleth-3 Phosphate, Phenoxyethanol, Butylene Glycol, Iodopropynyl Butylcarbamate, Triethoxycaprylylsilane

Elta MD UV Clear

Elta MD UV Clear

zinc oxide and octinoxate lotion LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:60232-2500
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 90 g
OCTINOXATE OCTINOXATE 75 g

Inactive Ingredients

Ingredient Name Strength
BUTYLENE GLYCOL
IODOPROPYNYL BUTYLCARBAMATE
PHENOXYETHANOL
water
CYCLOMETHICONE 5
NIACINAMIDE
OCTYLDODECYL NEOPENTANOATE
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)
TRIETHOXYCAPRYLYLSILANE
ALPHA-TOCOPHEROL ACETATE
OLETH-3 PHOSPHATE
LACTIC ACID
HYALURONATE SODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:60232-2500-1 1.7 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-07-01


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