Label: PERFECT SUN KIDS SUNSCREEN PROTECTOR AGAINST SOLAR RAYS FOR CHILDREN, FACE AND BODY SPF 50 FM- ensulizole, octinoxate, octisalate, octocrylene, oxybenzone, and titanium dioxide lotion
-
Contains inactivated NDC Code(s)
NDC Code(s): 13537-387-01, 13537-387-02 - Packager: Ventura Corporation LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated October 20, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
- Directions
- Other information
-
Inactive ingredients
WATER, DICAPRYLYL CARBONATE, VP/EICOSENE COPOLYMER, PHENETHYL BENZOATE, ARGININE, CYCLOHEXASILOXANE, CETEARYL ALCOHOL, SORBITAN STEARATE, DIMETHICONE, GLYCERYL STEARATE, POTASSIUM CETYL PHOSPHATE, TRIMETHYLSILOXYSILICATE, SILICA, DISODIUM LAURIMINODIPROPIONATE TOCOPHERYL PHOSPHATES, HYDROXYACETOPHENONE, METHYL METHACRYLATE CROSSPOLYMER, METHICONE, CETEARETH-20, 1,2 – HEXANEDIOL, CAPRYLYL GLYCOL, XANTHAN GUM, FRAGRANCE, CYCLOPENTASILOXANE.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 80 ml Bottle Label
-
INGREDIENTS AND APPEARANCE
PERFECT SUN KIDS SUNSCREEN PROTECTOR AGAINST SOLAR RAYS FOR CHILDREN, FACE AND BODY SPF 50 FM
ensulizole, octinoxate, octisalate, octocrylene, oxybenzone, and titanium dioxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-387 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Ensulizole (UNII: 9YQ9DI1W42) (Ensulizole - UNII:9YQ9DI1W42) Ensulizole 0.03 g in 1 mL Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.075 g in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 0.05 g in 1 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 0.07 g in 1 mL Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 0.06 g in 1 mL Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP) Titanium Dioxide 0.047 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) PHENETHYL BENZOATE (UNII: 0C143929GK) ARGININE (UNII: 94ZLA3W45F) CYCLOMETHICONE 6 (UNII: XHK3U310BA) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DISODIUM LAURIMINODIPROPIONATE TOCOPHERYL PHOSPHATES (UNII: 0K5Y9U1P6M) METHICONE (20 CST) (UNII: 6777U11MKT) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) XANTHAN GUM (UNII: TTV12P4NEE) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13537-387-02 1 in 1 BOX 1 NDC:13537-387-01 80 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 10/22/2015 Labeler - Ventura Corporation LTD (602751344) Establishment Name Address ID/FEI Business Operations Bel Star S.A. (Colombia) 880160197 MANUFACTURE(13537-387)