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Academy

ACADEMY, LTD

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients


Avobenzone    3.0%

Homosalate     13.0%

Octisalate        5.0%

Octocrylene     7.0%

Oxybenzone     4.0%



Purpose

Sunscreen


Academy 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.


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.


  • May stain some fabrics.

Directions

  • apply liberally 15 minutes before sun exposure
  • 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 of age: Ask a doctor.

Inactive ingredients

Water, Sorbitol, Stearic Acid, Triethanolamine, Aluminum Starch Octenylsuccinate, Benzyl Alcohol, Sorbitan Isostearate, VP/Eicosene Copolymer, Dimethicone, Polyglyceryl-3 Distearate, Carbomer, Tocopherol, Disodium EDTA, Methylparaben, Propylparaben, Fragrance


Principal Display Panel

Academy

SPORTS+OUTDOORS

SUNSCREEN LOTION

BROAD SPECTRUM SPF 50

50

Water Resistant

(80 Minutes)

Hypoallergenic

UVA/UVB Protection

8 FL. OZ.

(236 mL)



Academy

Academy Other information

  • protect this product from excessive heat and direct sun

Academy

AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59054-120
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 3 g
HOMOSALATE Homosalate 13 g
OCTISALATE OCTISALATE 5 g
OCTOCRYLENE Octocrylene 7 g
OXYBENZONE OXYBENZONE 4 g

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
STEARIC ACID
TROLAMINE
ALUMINUM STARCH OCTENYLSUCCINATE
BENZYL ALCOHOL
Sorbitan Isostearate
DIMETHICONE
POLYGLYCERYL-3 DISTEARATE
Tocopherol
EDETATE DISODIUM
METHYLPARABEN
PROPYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59054-120-16 226 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-06-28


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