Isomers Sunscreen with UV pearls Broad Spectrm SPF 20 description, usages, side effects, indications, overdosage, supplying and lots more!

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Isomers Sunscreen with UV pearls Broad Spectrm SPF 20

Isomers Laboratories Inc
Isomers Laboratories Inc

DRUG FACTS




FULL PRESCRIBING INFORMATION

Active ingredient

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Active Ingredients:

Zinc Oxide                           8.0%

Octyl Methoxycinnamate      7.5%

Purpose

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Purpose

Sunscreen

Uses

  • helps prevent sunburn
  • if used as directed with other sun protection measures (See Direction ),decreases the risk of skin cancer and early skin aging caused by the sun.
  • For external use only
  • When using this product, keep out of eyes.Rinse with watewr to remove.

Do Not Use on damaged or broken skin

Stop use and ask a doctor if rash occurs.

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  • Keep out of reach of children
  • If product is swallowed get medical help or contact the Poison Control Center right away.

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Inactive Ingredients:

Purified Water, Cetearyl Alcohol, Phenyl Trimethicone, Caprylic/Capric Triglyceride, Propylen Glycol, Ceteareth-20, Polyhydroxystearic Acid, Mineral Oil, Panthenol, Silica, PVP, Chlorphenesin, Tocopheryl Acetate, Aloe Barbadensis Leaf extract, Polysorbate 60, BHT, Phenoxyethanol, Disodium EDTA, Diazolidinyl Urea, Methylparaben, Propylparaben.

  • Apply Liberally 15 minutes before sun exposure.
  • reapply at least every two hours
  • use a water -resistant sunscreen if swimming or sweating
  • children under 6 months of age: Ask a doctor.
  • Sun protection measures: Spending time in the sun increases your risk of skin cancer and early skin aging.To decrease this risk, regulary use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures.
  • Limit time in the sun especially from 10 a.m. to 2 p.m.
  • wear long-sleeved shirts, pants, hats and sunglasses.

MM10 Isomers Sunscreen with UV pearls Broad Spectrm SPF 20

Isomers Sunscreen with UV pearls Broad Spectrm SPF 20

Zinc Oxide, Octinoxate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64990-885
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 80 mg
OCTINOXATE OCTINOXATE 75 mg

Inactive Ingredients

Ingredient Name Strength
water
CETOSTEARYL ALCOHOL
POLYSORBATE 60
MEDIUM-CHAIN TRIGLYCERIDES
SILICON DIOXIDE
CHLORPHENESIN
BUTYLATED HYDROXYTOLUENE
Aloe Vera Leaf
PANTHENOL
METHYLPARABEN
PROPYLPARABEN
PHENYL TRIMETHICONE
propylene glycol
POLYHYDROXYSTEARIC ACID (2300 MW)
Mineral Oil
.ALPHA.-TOCOPHEROL ACETATE
PHENOXYETHANOL
MAGNESIUM DISODIUM EDTA
UREA

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64990-885-01 120 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2003-03-31


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