DHC White Sunscreen description, usages, side effects, indications, overdosage, supplying and lots more!

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DHC White Sunscreen

DHC USA Incorporated

DHC White Sunscreen


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active Ingredients Purpose
titanium dioxide 5% Sunscreen
zinc oxide 10% Sunscreen

DHC White Sunscreen Uses

  • Helps prevent sunburn.
  • Higher SPF gives more sunburn protection.
  • Provides moderate protection against sunburn and tanning.

Warnings

For external use only.

When using this product

  • keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

  • rash or irritation develops and lasts.

Keep out of reach of children.

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Shake well. Apply evenly before sun exposure and as needed.
  • Children under 6 months of age: ask a doctor.
  • Reapply as needed or after towel drying, swimming, or perspiring.

Other Information

  • Moderate sun protection product.
  • Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Inactive Ingredients

cyclopentasiloxane, water, talc, dimethicone, PEG-10 dimethicone, triethylhexanoin, glycerin, nylon-12, methicone, pentylene glycol, olea europaea (olive) leaf extract, olea europaea (olive) fruit oil, PEG-9 polydimethylsiloxyethyl dimethicone, magnolia obovata bark extract, aluminum hydroxide, alpha-arbutin, zirconium dioxide, phenoxyethanol, tocopherol, aloe barbadensis leaf juice, pentasodium pentetate, tricalcium phosphate, ascorbyl tetraisopalmitate, citric acid, silica, silver

Questions or Comments?

1-800-DHC-CARE (342-2273)

www.dhccare.com

PRINCIPAL DISPLAY PANEL - 30 ml Carton

DHC

White
Sunscreen

SPF 25

1 fl. oz. (30 ml)

DHC White Sunscreen

DHC White Sunscreen

Titanium Dioxide and Zinc Oxide CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63433-451
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 50 mg
Zinc Oxide Zinc oxide 100 mg

Inactive Ingredients

Ingredient Name Strength
CYCLOMETHICONE 5
water
talc
DIMETHICONE
TRIETHYLHEXANOIN
GLYCERIN
PENTYLENE GLYCOL
Olea Europaea Leaf
olive oil
MAGNOLIA OBOVATA BARK
aluminum hydroxide
Zirconium Oxide
PHENOXYETHANOL
Tocopherol
Aloe Vera Leaf
PENTASODIUM PENTETATE
TRICALCIUM PHOSPHATE
CITRIC ACID MONOHYDRATE
SILICON DIOXIDE
SILVER

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63433-451-51 30 in 1 BOTTLE, PLASTIC
2 NDC:63433-451-79 1.5 in 1 CELLO PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2005-05-01


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