SPF15 sunscreen description, usages, side effects, indications, overdosage, supplying and lots more!

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SPF15 sunscreen

Yuyao Jessie Commodity Co.,Ltd.

SPF 15 sunscreen spray


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Octinoxate 4.0%
oxybenzone 4.0%
Octisalate 2.0%

Purpose

Sunscreen

Use

Use in well ventilated areas

WARNINGS

For External use only.
Not to be swallowed.Avoid contact with eyes.Discontinue use if signs of irritation or rash appear.Use on children under 6 months of age only with advice of a physician.Keep this and all drug out of the reach of children.In case of accidental ingestion,seek professional assistance or contact a Poision Control Center immediately

keep out of reach of children

Use on children under 6 months of age only with advice of a physician.Keep this and all drug out of the reach of children.

Directions

For best results ,apply 15-30 minutes before sun exposure ,Hold bottle 4-6 inches away from body and apply liberally,spraying slowly and evenly until product is visible on skin.can be applied diredtly to wet skin.reapply after swimming ,excessive perspiration,towel drying or extended sun exposure.Do not apply in windy conditions.Do not spray into face.Spray into hand and apply to the face.Use in well ventilated areas.

Inactive ingredients

ALCOHOL Denat,Glycerin ,Tocopherol ,Fragrance,Deionized WATER ,POLYSORBATE 20

lebel

SPF15 sunscreen

SPF15 sunscreen

Octinoxate,oxybenzone,OCTISALATE SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51414-600
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 4 g
OXYBENZONE OXYBENZONE 4 g
OCTISALATE OCTISALATE 2 g

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
GLYCERIN
Tocopherol
water
POLYSORBATE 20

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51414-600-01 5 in 1 PACKAGE
2 NDC:51414-600-02 7 in 1 PACKAGE
3 NDC:51414-600-03 8 in 1 PACKAGE
4 NDC:51414-600-04 10 in 1 PACKAGE
5 NDC:51414-600-05 12 in 1 PACKAGE
6 NDC:51414-600-06 15 in 1 PACKAGE
7 NDC:51414-600-07 20 in 1 PACKAGE
8 NDC:51414-600-08 25 in 1 PACKAGE
9 NDC:51414-600-09 30 in 1 PACKAGE
10 NDC:51414-600-10 40 in 1 PACKAGE
11 NDC:51414-600-11 50 in 1 PACKAGE
12 NDC:51414-600-12 60 in 1 PACKAGE
13 NDC:51414-600-13 70 in 1 PACKAGE
14 NDC:51414-600-14 80 in 1 PACKAGE
15 NDC:51414-600-15 90 in 1 PACKAGE
16 NDC:51414-600-16 100 in 1 PACKAGE
17 NDC:51414-600-17 120 in 1 PACKAGE
18 NDC:51414-600-18 130 in 1 PACKAGE
19 NDC:51414-600-19 150 in 1 PACKAGE
20 NDC:51414-600-20 160 in 1 PACKAGE
21 NDC:51414-600-21 180 in 1 PACKAGE
22 NDC:51414-600-22 200 in 1 PACKAGE
23 NDC:51414-600-23 220 in 1 PACKAGE
24 NDC:51414-600-24 250 in 1 PACKAGE
25 NDC:51414-600-25 300 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-09-12


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