ELTAMD UV SPORT SPF50- zinc oxide, octinoxate and octisalate sunscreen lotion 
CP Skin Health Group, Inc.

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EltaMD UV Sport SPF50

Warnings

For external use only Do not use on damaged or broken skin When suing this product keep out of eyes. Rinse with water to remove. Stop use and ask physician if rash occurs Keep out of reach of children. If product is swallowed contact a Poison Control Center right away.

Active ingredients

Zinc Oxide 9.0%   Sunscreen
Octinoxate 7.5%   Sunscreen
Octisalate 5.0%   Sunscreen

Uses

Helps prevent sunburn If used as directed withother sun protection measures (See Directions) decreases the risk of skin cancer and early skin aging caued by the sun.

Directions

Apply liberally 15 minutes before sun exposure Reapply after 80 minutes of swimming or sweating immedaitely after towel drying at least every 2 hours Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10a.m.-2p.m. wear long-sleeve shirts, pants, hats and sunglasses Children under 6 months: Ask a physician

Doseage and administration

Apply liberally 15 minutes before sun exposure Reapply after 80 minutes of swimming or sweating immedaitely after towel drying at least every 2 hours

Inactive ingredients

Beeswax, Butylene Glycol, Cetyl Dimethicone, Cetyl PEG/PPG-10/ 1 Dimethicone, Disodium EDTA, Hexyl Laurate, Hydrogenated Castor Oil, Iodopropynyl Butylcarbamate, Isopropyl Palmitate, Octyldoceyl Neopentaoate, Polyglyceryl-4 Isostearate, Purified Water, Sodium Chloride, Tocopheryl Acetate, Triethoxycaprylylsilane

Keep out of reach of children

Keep out of reach of children

Labeling

UV Sport 3oz UC

ELTAMD UV SPORT SPF50 
zinc oxide, octinoxate and octisalate sunscreen lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72043-2287
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION90 g  in 1000 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 g  in 1000 g
octisalate (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) octisalate50 g  in 1000 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)  
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
HEXYL LAURATE (UNII: 4CG9F9W01Q)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72043-2287-384 g in 1 TUBE; Type 0: Not a Combination Product01/10/2018
2NDC:72043-2287-9226 g in 1 TUBE; Type 0: Not a Combination Product05/30/2024
3NDC:72043-2287-8198 g in 1 BOTTLE; Type 0: Not a Combination Product01/10/201805/30/2024
4NDC:72043-2287-22 g in 1 PACKET; Type 0: Not a Combination Product07/07/2022
5NDC:72043-2287-61815 g in 1 BOTTLE; Type 0: Not a Combination Product07/07/202209/11/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/10/2018
Labeler - CP Skin Health Group, Inc. (611921669)
Registrant - Swiss-American CDMO, LLC (080170933)
Establishment
NameAddressID/FEIBusiness Operations
Swiss-American CDMO, LLC080170933manufacture(72043-2287)

Revised: 5/2024
Document Id: 872ddab8-70ef-4efc-91d9-529816ce80cb
Set id: dffc3fde-5b6e-4a62-8289-9733be43455b
Version: 8
Effective Time: 20240530
 
CP Skin Health Group, Inc.