Glytone Suncare block sunscreen description, usages, side effects, indications, overdosage, supplying and lots more!

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Glytone Suncare block sunscreen

Genesis Pharmaceutical

Glytone suncare block sunscreen




FULL PRESCRIBING INFORMATION

Inactive Ingredients Water USP, Isopropyl Myristate, Octyldoceyl Neopentanoate, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Polysorbate 60, Diethanolamine Cetyl Phosphate, Hyaluronic Acid, Polyether-1, Galactoarabinan, Polyacrylamide, C13-14 isoparaffin, Laureth-7, Triethoxycaprylylsilane, Sodium Hydroxide, Citric Acid, Phenoxyethanol, Methylparaben, Propylparaben, Disodium EDTA

Active ingredient



Active Ingredients                                       Purpose

Octinoxate 7.5%                                             Sunscreen

Octisalate 2%                                                  Sunscreen

Zinc Oxide 7.5%                                             Sunscreen

Purpose




Directions

For sunscreen use

Apply liberally and evenly 15  minutes before sun exposure

Use a water resistant sunscreen if swimming or sweating

Reapply every two hours

Apply to all skin exposed to the sun

Children under 6 months: 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, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 am- 2 pm., wear long-sleeved shirts, pants, hats and sunglasses



Warnings










Keep away from children.


Uses






Other Information

Protect the product in this container from excessive heat and direct sun

Questions Call 1-800-459-8663


Glytone Suncare block sunscreen

Glytone

Suncare

block

sunscreen lotion

SPF 40

UVA/UVB

PABA-FREE

FRANGRANCE-FREE

NON-IRRITATING

OIL-FREE

NON COMEDOGENIC

MINERAL BASED (WITH MICRONIZED ZINC OXIDE)

120 ml/ 4 fl oz.

Glytone Suncare block sunscreen

octinoxate, octisalate, xinc oxide LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64760-215
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 9 mL
OCTISALATE OCTISALATE 2.4 mL
Zinc Oxide Zinc oxide 9 mL

Inactive Ingredients

Ingredient Name Strength
water
ISOPROPYL MYRISTATE
OCTYLDODECYL NEOPENTANOATE
MEDIUM-CHAIN TRIGLYCERIDES
CETOSTEARYL ALCOHOL
POLYSORBATE 60
DIETHANOLAMINE CETYL PHOSPHATE
HYALURONIC ACID
C13-14 ISOPARAFFIN
LAURETH-7
SODIUM HYDROXIDE
CITRIC ACID MONOHYDRATE
PHENOXYETHANOL
METHYLPARABEN
PROPYLPARABEN
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 120 in 1 TUBE
2 NDC:64760-215-02 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-06-25


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