glytone retexturize hand description, usages, side effects, indications, overdosage, supplying and lots more!

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glytone retexturize hand

Genesis Pharmaceuticals

Glytone retexturize hand




FULL PRESCRIBING INFORMATION

Active ingredient


Active Ingredients                  Purpose

Octinoxate 6.0%                        Sunscreen

Octisalate 3.0%                           Sunscreen

Oxybenzone 5.0%                     Sunscreen




Inactive Ingredients

Water (Aqua), Glycolic Acid, Cyclomethicone, Glyceryl Stearate, Polyacrylamide, Boron Nitride, Butylene Glycol, Ethylhexly Palmitate, Persea Gratissima (Avocado) Oil Unsaponifiables, Ammoniium Hydroxide, C13-14 Isoparaffin, Stearly Alcohol, Dimethiconol, Laureth-7, Magnesium Nitrate, Disodium EDTA, Tocopheryl Acetate, Methyl-chloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone.

Uses



Uses

Helps prevent sunburn

Higher SPF gives more sunburn protection

Porvides moderate protection against sunburn



Warnings

For external use only

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.

This product is not intended for sunbathing.



Directions

Apply once or twice a day or as directed by your doctor; avoid face.

Apply generously before sun exposure and as needed.

Children under 6 months of age: ask a doctor.


glytone retexturize hand

Glytone Body

retexturize hand cream SPF 15

glycolic complex

120 mL E/4 Fl. Oz.

glytone retexturize hand

octinoxate, octisalate, oxybenzone CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64760-207
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 7.2 mm
OCTISALATE OCTISALATE 3.6 mL
OXYBENZONE OXYBENZONE 6 mL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64760-207-01 120 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-05-24


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