Elta MD UV SPF46 description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Elta MD UV SPF46

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

Elta MD UV Spray SPF46




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients        Purpose

Zinc Oxide 9.3%         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 this product keep out of eyes.  Rinse with water to remove.
  • Top 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.
  • Hard surfaces may become damp when product is sprayed.  Avoid slips or falls.

Directions

  • Shake Well before use
  • apply liberally 15 minutes before sun exposure.  Gently rub in.
  • reapply
    • after 80 minutes of swimming or sweating
    • immediately after towel drying
    • 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

Butylene Glycol, Capryloyl Glycine, Cyclopentasiloxane, Dimethicone, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Lauryl PEG-9 Polymethylsiloxyethyl Dimethicone, Phenoxyethanol, Purified Water, Sodium Chloride, Triethoxycaprylylsilane, Undecylenoyl Glycine

Elta MD UV SPF46

Elta MD UV SPF46

zinc oxide and octinoxate sunscreen SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:60232-2585
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 93 g
OCTINOXATE OCTINOXATE 75 g

Inactive Ingredients

Ingredient Name Strength
BUTYLENE GLYCOL
PHENOXYETHANOL
Capryloyl Glycine
UNDECYLENOYL GLYCINE
CYCLOMETHICONE 5
water
SODIUM CHLORIDE
TRIETHOXYCAPRYLYLSILANE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:60232-2585-4 4 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-06-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.