Duane Reade Sunscreen description, usages, side effects, indications, overdosage, supplying and lots more!

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Duane Reade Sunscreen

DUANE READE INC.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Avobenzone 3.0 %

Homosalate 15.0%

Octisalate 5.0%

Octocrylene 10.0%

Oxybenzone 6.0%

Purpose

Sunscreen

Duane Reade Sunscreen Uses

  • helps prevent sunburn
  • higher SPF gives more sunburn protection
  • retains SPF after 80 minutes of activity in the water

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 generously and evenly before sun exposure and as needed
  • children under 6 months of age:ask a doctor
  • reapply frequently and after towel drying, swimming or perspiring

Other Information

  • may stain some materials
  • Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin agin, skin cancer, and other harmful effects of the sun.

Inactive Ingredients

Water, Glyceryl Stearate, Microcrystalline Cellulose, Butylene Glcyol, PEG_100 Stearate, Benzyl Alcohol, Acrylates/C12-22 Alkyl Methcrylate Copolymer, Diethylhexyl Syringylidenemalonate, Behenyl Alcohol, Butylated PVP, Palmitic Acid, Lecithin, Stearic Acid, Cellulose Gum, Myristyl Alcohol, Caprylic/Capric Triglyceride, Tocopherol, Retinyl Palmitate, Disodium EDTA, Sodium Ascorbyl Phosphate, Cetyl Alcohol, Lauryl Alcohol, Chlorphenesin.

Principal Display Panel

UNIQUELY NY DRTM SINCE 1960

sunscreen

70

SPF

moisturizing lotion

Photostable

Broad Spectrum

UVA/UVB Protection

Very Water Resistant

8 FL.OZ.(237 mL)Duane Reade Sunscreen Duane Reade Sunscreen

Duane Reade Sunscreen

AVOBENZONE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67732-409
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 3 g
HOMOSALATE Homosalate 15 g
OCTISALATE OCTISALATE 5 g
OCTOCRYLENE Octocrylene 10 g
OXYBENZONE OXYBENZONE 6 g

Inactive Ingredients

Ingredient Name Strength
water
GLYCERYL MONOSTEARATE
STEARIC ACID
cellulose, microcrystalline
BUTYLENE GLYCOL
PEG-100 STEARATE
BENZYL ALCOHOL
Diethylhexyl Syringylidenemalonate
docosanol
PALMITIC ACID
CARBOXYMETHYLCELLULOSE SODIUM
Tocopherol
EDETATE DISODIUM
MYRISTYL ALCOHOL
TRICAPRYLIN
VITAMIN A PALMITATE
SODIUM ASCORBYL PHOSPHATE
CETYL ALCOHOL
Lauryl Alcohol
CHLORPHENESIN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:67732-409-16 226 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-11-14


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