Rayito de Sol Sunscreen SPF 6 description, usages, side effects, indications, overdosage, supplying and lots more!

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Rayito de Sol Sunscreen SPF 6

Siscom de Argentina SA

Rayito de Sol Sunscreen SPF 6


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Octisalate 4%

Oxybenzone 1%

Purpose

Sunscreen

Sunscreen

Rayito de Sol Sunscreen SPF 6 Uses

  • Helps prevent sunburn.
  • Higher SPF gives more sunburn protection.
  • Provides minimal protection against sunburn.

Warnings

For external use only.

When using this product

  • do not use in or near the eyes
  • if it gets into eyes rinse thoroughly with water

Stop use and ask a doctor if

  • rash or irritation develops and lasts
Side effect occur. You may report side effects to FDA at 1-800-FDA-1088

If swallowed, seek medical attention or contact a Poison Control Center immediately.

Keep out of the reach of children


Directions

  • Apply generously 15 minutes before sun exposure.
  • Children under six months of age: ask a doctor.
  • Reapply every 2 hours or after swimming or sweating or anytime after towelling.

Other Information

  • Minimal sun protection product.
  • Sun alert: limiting sun exposure, wearing protective clothing, and using sunscreens my reduce the risk of skin aging, skin cancer and other harmful effects of the sun.
  • May stain clothing when freshly applied. Avoid contact with fabric or if fabric contact, launder within the hour.

Inactive ingredients

Mineral Oil, Petrolatum, Propylene Glycol, Ceresin, Paraffin, CI 77492 (and) CI 77491 (and) CI 77499, Zinc Stearate, Cera Alba, Fragrance, Propylparaben, Benzyl Salicylate, Benzyl Alcohol, Hydroxycitronellal, Linalool, Coumarin, Citronellol, Geraniol, Eugenol, Amyl Cinnamal, Isoeugenol.

Questions or comments?

if you are in United States

(305) 672-9486

Principal Display Panel







Rayito de Sol Sunscreen SPF 6


Rayito de Sol Sunscreen SPF 6

Octisalate Oxybenzone CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:20367-111
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTISALATE OCTISALATE 2.8 g
OXYBENZONE OXYBENZONE 0.7 g

Inactive Ingredients

Ingredient Name Strength
Mineral Oil
petrolatum
propylene glycol
Ceresin
PARAFFIN
ZINC STEARATE
YELLOW WAX
PROPYLPARABEN
BENZYL SALICYLATE
BENZYL ALCOHOL
Hydroxycitronellal
LINALOOL, DL-
Coumarin
.BETA.-CITRONELLOL, (+/-)-
GERANIOL
Eugenol
.ALPHA.-AMYLCINNAMALDEHYDE
Isoeugenol
FERRIC OXIDE YELLOW
ferric oxide red
FERROSOFERRIC OXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 70 in 1 TUBE
2 NDC:20367-111-01 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-02-14


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