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Ulta

Prime Packaging, Inc.
Prime Packaging, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

PRINCIPAL DISPLAY PANEL - 177 mL Can Label

Ulta

ULTA

OIL-FREE

SUNSCREEN

CONTINUOUS SPRAY

SPF 15

WATER RESISTANT (80 MINUTES)

NON-GREASY FORMULA

SUNSPORT

6 FL.OZ/177 mL.

Active ingredients

Avobenzone 2 %, Octisalate 5 %, and Octocrylene 2.75 %

Purpose

Purpose

Sunscreen

Ulta Uses

  • 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 prevent sunburn, not skin cancer or early skin aging.

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. Keep away from face to avoid breathing it. Contents under pressure - do not puncture or incinerate. Do not store at temperatures above 1200F

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.

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

Directions

  • spray liberally and spread by hand 15 minutes before sun exposure
  • hold container 4 to 6 inches from the skin to apply
  • do not spray directly into face. Spray on hands then apply to face.
  • do not apply in windy conditions
  • use in well-ventilated areas.
  • reapply:
    • after 80 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours
  • children under 6 months: Ask a doctor

Inactive Ingredients

Acrylates/Octylacrylamide Copolymer, Butyloctyl Salicylate, Diethylhexyl 2,6-Naphthalate, Fragrance (Parfum), Polyester-8, SD Alcohol 40-B

Ulta Other information

  • protect this product from excesive heat and direct sun
  • avoid spraying on fabrics - could cause discoloration

Questions or Comments?

Call toll free 1-800-983-8582

Ulta

Avobenzone, Octisalate, and Octocrylene SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:13630-0043
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 16.7 mg
OCTISALATE OCTISALATE 41.8 mg
OCTOCRYLENE Octocrylene 22.9 mg

Inactive Ingredients

Ingredient Name Strength
BUTYLOCTYL SALICYLATE
Diethylhexyl 2,6-Naphthalate
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED)
ALCOHOL

Product Characteristics

Color
yellow

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:13630-0043-4 177 in 1 CAN

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2008-11-26


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