CoreTex Sun X SPF 30 description, usages, side effects, indications, overdosage, supplying and lots more!

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CoreTex Sun X SPF 30

CoreTex Products

Sun X SPF 30 Lotion


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Avobenzone 1.0%

Homosalate 5.0%

Octinoxate 7.5%

Octisalate 5.0%

Oxybenzone 6.0%

Purpose

Sunscreen

Sunscreen

Sunscreen

Sunscreen

Sunscreen

CoreTex Sun X SPF 30 Uses

helps prevent sunburn

If used as directed with other sun protection measures  (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only

Do not use

  • on damaged or broken skin

When using this product

  • keep out of the eyes
  • rinse with water to remove

Stop use and ask a doctor if

  • rash occurs

Keep out of the reach of children

If swallowed get medical help or contact  a Poison Control center right away.

Directions

  • apply liberally  and evenly 15 minutes before sun exposure
  • 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 after sun protection measures including:
  • limit time in the sun, especially from 10:00 a.m. - 2 p.m.
  • wear long-sleeved shirts, pants, hats and sunglasses.
  •  reapply:
    • after 80 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours
  • children under 6 months of age: Ask a doctor

CoreTex Sun X SPF 30 Other information

  • protect this product from excessive heat or direct sun

Inactive ingredients

acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, butylparaben, calendula officinalis flower extract, carbomer, chamomile recutita extract, dimethicone, dimethyl capramide,  ethylparaben, fragrance,  glyceryl stearate, isobutylparaben, methylparaben, nasturtium officinale extract, peg-100 stearate, phenoxyethanol, propylparaben, symphytum officinale leaf extract, tetrasodium EDTA, triethanolamine, tocopherol, tocopherol acetate, water

Questions?

Call 1-877-684-5774

Principal Display Panel

image of pdpCoreTex Sun X SPF 30

CoreTex Sun X SPF 30

Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65753-100
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 1 g
HOMOSALATE Homosalate 5 g
OCTINOXATE OCTINOXATE 7.5 g
OCTISALATE OCTISALATE 5.0 g
OXYBENZONE OXYBENZONE 6 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHYL CAPRAMIDE
DIMETHICONE
Aloe Vera Leaf
.ALPHA.-TOCOPHEROL
TROLAMINE
PROPYLPARABEN
PHENOXYETHANOL
GLYCERYL MONOSTEARATE
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
isobutylparaben
C12-15 ALKYL BENZOATE
CHAMOMILE
CALENDULA OFFICINALIS FLOWER
PEG-100 STEARATE
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
NASTURTIUM OFFICINALE
COMFREY LEAF
EDETATE SODIUM
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)

Product Characteristics

Color
white (Thick White Lotion)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65753-100-01 30 in 1 BOTTLE, PLASTIC
2 NDC:65753-100-32 44 in 1 BOTTLE, PLASTIC
3 NDC:65753-100-02 59 in 1 BOTTLE, PLASTIC
4 NDC:65753-100-33 59 in 1 BOTTLE, PLASTIC
5 NDC:65753-100-03 118 in 1 BOTTLE, PLASTIC
6 NDC:65753-100-34 118 in 1 BOTTLE, PLASTIC
7 NDC:65753-100-04 177 in 1 BOTTLE, PLASTIC
8 NDC:65753-100-05 236 in 1 BOTTLE, PLASTIC
9 NDC:65753-100-07 473 in 1 BOTTLE, PLASTIC
10 NDC:65753-100-09 946 in 1 BOTTLE, PLASTIC
11 NDC:65753-100-10 3785 in 1 BOTTLE, PLASTIC
12 NDC:65753-100-37 44 in 1 PACKET
13 44 in 1 PACKET
14 207 in 1 PACKET
15 207 in 1 PACKET
16 207 in 1 PACKET
17 207 in 1 PACKET
18 207 in 1 PACKET
19 500 in 1 BAG
20 NDC:65753-100-08 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-01-25


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