SKINPROTECT SPF 50 SHEER ROLLER SUNSCREEN- homosalate, octinoxate, octocrylene, octisalate, avobenzone lotion 
Mitchell Group USA, LLC

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SkinProtect SPF 50 SHEER ROLLER SUNSCREEN

Drug Facts

SkinProtect Sheer SPF

Active Ingredients

Homosalate 10.00%
Octinoxate 7.50%
Octocrylene 7.50%
Octisalate 5.00%
Avobenzone 3.00%

Purpose

Sunscreen

Uses:

Screens out sun’s burning rays to help prevent sunburn.

Warnings:

For external use only.

Keep out of reach of children.

Sun Alert: UV exposure from the sun increases the risk of skin cancer, premature skin aging. Decrease UV exposure by limiting time in the sun, wearing protective clothing and using a sunscreen.

Avoid contact with eyes.
Rinse with water to remove.

Stop use and ask a doctor

if skin rash develops.

Other information:

store in cool dry place.

Ingredients:

Aqua (Deionized Water), C12-15 Alkyl Benzoate, Carbomer, Cetyl Alcohol, Cocos Nucifera (Coconut) Oil, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Hyaluronic Acid, Parfum (Fragrance), PEG-100 Stearate, Phenoxyethanol, Polysorbate-20, Potassium Hydroxide, Propylene Glycol, Stearyl Alcohol, Tocopheryl Acetate (Vitamin E),

Package Labeling:

Label

SKINPROTECT SPF 50 SHEER ROLLER SUNSCREEN 
homosalate, octinoxate, octocrylene, octisalate, avobenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71636-841
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
COCONUT OIL (UNII: Q9L0O73W7L)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
HYALURONIC ACID (UNII: S270N0TRQY)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71636-841-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product08/03/201711/30/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02008/03/201711/30/2019
Labeler - Mitchell Group USA, LLC (825444685)

Revised: 10/2023
Document Id: 074ba069-b691-bad7-e063-6394a90ac4be
Set id: 55ddafc3-41b8-3566-e054-00144ff88e88
Version: 2
Effective Time: 20231009
 
Mitchell Group USA, LLC