SPF15 SUNSCREEN- octinoxate, oxybenzone and octisalate spray 
Yuyao Jessie Commodity Co.,Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.


SPF 15 sunscreen spray

Active Ingredient

Octinoxate 4.0%
oxybenzone 4.0%
Octisalate 2.0%




Use in well ventilated areas


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.


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



octinoxate,oxybenzone,octisalate spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:51414-600
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate 4 g  in 100 g
oxybenzone (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) oxybenzone 4 g  in 100 g
Octisalate (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) Octisalate 2 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
ALCOHOL (UNII: 3K9958V90M)  
glycerin (UNII: PDC6A3C0OX)  
tocopherol (UNII: R0ZB2556P8)  
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51414-600-01 5 g in 1 PACKAGE
2 NDC:51414-600-02 7 g in 1 PACKAGE
3 NDC:51414-600-03 8 g in 1 PACKAGE
4 NDC:51414-600-04 10 g in 1 PACKAGE
5 NDC:51414-600-05 12 g in 1 PACKAGE
6 NDC:51414-600-06 15 g in 1 PACKAGE
7 NDC:51414-600-07 20 g in 1 PACKAGE
8 NDC:51414-600-08 25 g in 1 PACKAGE
9 NDC:51414-600-09 30 g in 1 PACKAGE
10 NDC:51414-600-10 40 g in 1 PACKAGE
11 NDC:51414-600-11 50 g in 1 PACKAGE
12 NDC:51414-600-12 60 g in 1 PACKAGE
13 NDC:51414-600-13 70 g in 1 PACKAGE
14 NDC:51414-600-14 80 g in 1 PACKAGE
15 NDC:51414-600-15 90 g in 1 PACKAGE
16 NDC:51414-600-16 100 g in 1 PACKAGE
17 NDC:51414-600-17 120 g in 1 PACKAGE
18 NDC:51414-600-18 130 g in 1 PACKAGE
19 NDC:51414-600-19 150 g in 1 PACKAGE
20 NDC:51414-600-20 160 g in 1 PACKAGE
21 NDC:51414-600-21 180 g in 1 PACKAGE
22 NDC:51414-600-22 200 g in 1 PACKAGE
23 NDC:51414-600-23 220 g in 1 PACKAGE
24 NDC:51414-600-24 250 g in 1 PACKAGE
25 NDC:51414-600-25 300 g in 1 PACKAGE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 09/12/2012
Labeler - Yuyao Jessie Commodity Co.,Ltd. (529892305)
Name Address ID/FEI Business Operations
Yuyao Jessie Commodity Co.,Ltd. 529892305 manufacture(51414-600)

Revised: 11/2012
Document Id: 2c7c503c-c846-4e56-b23b-0481a8b57002
Set id: 8c9374ae-2522-4f98-99c3-90ce82657bb6
Version: 3
Effective Time: 20121115
Yuyao Jessie Commodity Co.,Ltd.