Coppertone Dry description, usages, side effects, indications, overdosage, supplying and lots more!

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Coppertone Dry

MSD Consumer Care, Inc.

Coppertone Dry OilSPF 10


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients

Homosalate 5%, Octinoxate 7.5%, Octisalate 5% and Oxybenzone 3%

Purpose

Sunscreen

Use

helps prevent sunburn

Warnings

Skin Cancer/Skin Aging Alert

Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

For external use only

Flammable

Do not use near heat, flame, or while smoking.

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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • apply liberally 15 minutes before sun exposure
  • do not spray directly on face. Spray into hands and apply to face
  • reapply:
    • after 80 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours
  • children under 6 months: Ask a doctor

Other Information

  • protect this product from excessive heat and direct sun
  • may stain or damage some fabrics or surfaces
  • avoid long term storage above 40°C (104°F)

Inactive Ingredients

alcohol denat. (80.6% V/V), acrylates/octylacrylamide copolymer, mineral oil, fragrance

Questions?

866-288-3330

Distributed by MSD Consumer Care, Inc., PO Box 377, Memphis, TN 38151 USA, a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ USA.

PRINCIPAL DISPLAY PANEL - 177 mL Bottle Label

Coppertone ®
Tanning
Dry Oil
Pump Spray

SPF 10
Classic Scent
Sunscreen

Enjoy Instant
Radiance

Ultra Light
Water Resistant
(80 minutes)

6 FL OZ (177 mL)

28640-FB

Coppertone Dry

Coppertone Dry

Homosalate, Octinoxate, Octisalate, and Oxybenzone OIL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11523-7340
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HOMOSALATE Homosalate 42.2 mg
OCTINOXATE OCTINOXATE 63.3 mg
OCTISALATE OCTISALATE 42.2 mg
OXYBENZONE OXYBENZONE 25.32 mg

Inactive Ingredients

Ingredient Name Strength
Mineral Oil

Product Characteristics

Color
YELLOW (clear to pale yellow)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11523-7340-1 177 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-02-01


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