SPF 30 Sunscreen description, usages, side effects, indications, overdosage, supplying and lots more!

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SPF 30 Sunscreen

Hangzhou Haorun Technology CO.,LTD.

SPF 30 Sunscreen Spray


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Octinoxate 6.0%

Oxybenzone 4.0%

Octisalate 5.0%

Purpose

sunscreen

Use

Protection from the sun’s damaging effects.

Warnings

For external use only.Not to be swallowed.Avid contact with eyes.Discontinue use if signs  or 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 assisitance or contact and Poision Control Center imdediately.

Do not use near fire,Store at temerature below 120F(48).Use only as directed.intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Direction

For best results,apply 15-30 minutes befroes 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 directly to wet skin.Reapply after swimming,excessive perspiration,towel drying or extended sunexposure .Don not apply in windy conditions.Do not spray into face,Spray into hand and apply to the face.Use in well ventilated areas.

Inactive Ingredient

Alcohal Denat,Glycerin,Tocopherol,Fragrance,Deionized Water,Polysorbate-20

SPF 30 Sunscreen

SPF 30 Sunscreen

OCTINOXATE OXYBENZONE Octisalate SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57817-300
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 6 g
OXYBENZONE OXYBENZONE 4 g
OCTISALATE OCTISALATE 5 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:57817-300-01 10 in 1 BOTTLE
2 NDC:57817-300-02 12 in 1 BOTTLE
3 NDC:57817-300-03 15 in 1 BOTTLE
4 NDC:57817-300-04 20 in 1 BOTTLE
5 NDC:57817-300-05 25 in 1 BOTTLE
6 NDC:57817-300-06 30 in 1 BOTTLE
7 NDC:57817-300-07 35 in 1 BOTTLE
8 NDC:57817-300-08 40 in 1 BOTTLE
9 NDC:57817-300-09 45 in 1 BOTTLE
10 NDC:57817-300-10 50 in 1 BOTTLE
11 NDC:57817-300-11 60 in 1 BOTTLE
12 NDC:57817-300-12 70 in 1 BOTTLE
13 NDC:57817-300-13 80 in 1 BOTTLE
14 NDC:57817-300-14 90 in 1 BOTTLE
15 NDC:57817-300-15 100 in 1 BOTTLE
16 NDC:57817-300-16 110 in 1 BOTTLE
17 NDC:57817-300-17 120 in 1 BOTTLE
18 NDC:57817-300-18 150 in 1 BOTTLE
19 NDC:57817-300-19 180 in 1 BOTTLE
20 NDC:57817-300-20 200 in 1 BOTTLE
21 NDC:57817-300-21 250 in 1 BOTTLE
22 NDC:57817-300-22 300 in 1 BOTTLE
23 NDC:57817-300-23 2 in 1 PACKAGE
24 NDC:57817-300-23 2 in 1 PACKAGE
25 NDC:57817-300-24 3 in 1 PACKAGE
26 NDC:57817-300-25 4 in 1 PACKAGE
27 NDC:57817-300-26 5 in 1 PACKAGE
28 NDC:57817-300-27 6 in 1 PACKAGE
29 NDC:57817-300-28 7 in 1 PACKAGE
30 NDC:57817-300-29 8 in 1 PACKAGE
31 NDC:57817-300-30 9 in 1 PACKAGE
32 NDC:57817-300-31 10 in 1 PACKAGE
33 NDC:57817-300-32 12 in 1 PACKAGE
34 NDC:57817-300-33 15 in 1 PACKAGE
35 NDC:57817-300-34 20 in 1 PACKAGE
36 NDC:57817-300-35 25 in 1 PACKAGE
37 NDC:57817-300-36 30 in 1 PACKAGE
38 NDC:57817-300-37 35 in 1 PACKAGE
39 NDC:57817-300-38 40 in 1 PACKAGE
40 NDC:57817-300-39 45 in 1 PACKAGE
41 NDC:57817-300-40 50 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-04-18


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