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

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Sunscreen Wipe

KGP Products, Inc. (dba PREMIER)
ITW Dymon




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient                                                                                                          Purpose

Homosalate (2%)..........................................................................................................Sunscreen

Octinoxate (7.5%).........................................................................................................Sunscreen

Octisalate (4%).............................................................................................................Sunscreen

Oxybenzone (5%)........................................................................................................Sunscreen

Purpose

Uses

  • Provides high protection against sunburn.
  • Retains SPF after 80 minutes of sweating or activity in the water.

Warnings

For external use only.

Flammable.  Keep away from heat and flame when applying this product.

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

  • Unfold towel.
  • Apply evenly before sun exposure.
  • For children under 6 months, consult a doctor.
  • Reapply after towel drying, swimming or sweating.

Inactive Ingredients

Acrylates/Octylacrylamide Copolymer, Ethanol, Fragrance

Sunscreen Wipe

Sunscreen Wipe

HOMOSALATE OCTINOXATE OCTISALATE OXYBENZONE CLOTH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52648-6175
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HOMOSALATE Homosalate 20 g
OCTINOXATE OCTINOXATE 75 g
OCTISALATE OCTISALATE 40 g
OXYBENZONE OXYBENZONE 50 g

Inactive Ingredients

Ingredient Name Strength
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52648-6175-1 9 in 1 PACKET

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-09-28


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