Desert Essence Mineral Sunscreen SPF 35 description, usages, side effects, indications, overdosage, supplying and lots more!

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Desert Essence Mineral Sunscreen SPF 35

Autumn Harp, Inc.

Desert Essence Mineral Sunscreen SPF 35


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Zinc Oxide (15%)

Sunscreen

  • 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

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 a doctor if rash occurs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • apply liberally 15 minutes before sun sxposure
  • 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 Broad Spectrum SPF 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. - 2 p.m. Wear long sleeved shirts, pants, hats, and sunglasses
  • children under 6 months: ask a doctor
  • protect this product container from excessive heat and direct sun

Ethyl Palmate, Aloe Barbadensis Leaf Juice, Helianthus Annuus (Sunflower) Seed Oil, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter), Beeswax (Cera Alba), Anthemis Nobilis Flower Oil (Chamomile), Punica Granatum Extract (Pomegranate), Punica Granatum Fruit Juice (Pomegranate), Tocopherol (Vitamin E), Glycerin (Palm), Gluconolactone, Sodium Benzoate, Maltodextrin, Silica.

Principal Display Panel

image componentsDesert Essence Mineral Sunscreen SPF 35

Desert Essence Mineral Sunscreen SPF 35

Zinc Oxide CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51514-0236
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 15 g

Inactive Ingredients

Ingredient Name Strength
water
SORBITAN OLIVATE
SHEA BUTTER
GLUCONOLACTONE
GLYCERIN
SODIUM BENZOATE
Tocopherol
ALOE
Calcium Gluconate
POMEGRANATE JUICE
maltodextrin
SOYBEAN OIL
SILICON DIOXIDE
YELLOW WAX
POMEGRANATE
SUNFLOWER OIL
CHAMOMILE FLOWER OIL
Ethyl Palmitate
ETHYL OLEATE
ETHYL LINOLEATE

Product Characteristics

Color
white

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51514-0236-1 88.7 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-07-15


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