Scrubs Sunscren by ITW Pro Brands / Prime Enterprises / Lico Industries SCRUBS Sunscreen Lotion

Scrubs Sunscren by

Drug Labeling and Warnings

Scrubs Sunscren by is a Otc medication manufactured, distributed, or labeled by ITW Pro Brands, Prime Enterprises, Lico Industries. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SCRUBS SUNSCREN- sunscreen lotion 
ITW Pro Brands

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SCRUBS Sunscreen Lotion

Active Ingredients

Active Ingredients

Purpose

Sunscreen

Sunscreen

Sunscreen

Sunscreen

Uses

  • helps prevent sunburn.
  • higher SPF gives more sunburn protection.
  • retains SPF after 80 minutes of water or sweating.
  • provides high protection against sunburn.

Warnings

For external use only.

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

Stop use and ask a doctor rash or irritation develops and lasts

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure

reapply

  • after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours

Other Information

Protect this product from excessive heat and direct sun.

Sun alert: Limiting exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.

Inactive Ingredients

Inactive Ingredients

Questions and comments?

Call: 1-877-684-5774

Package Label

Sunscreen

SCRUBS SUNSCREN 
sunscreen lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 51239-3921
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE0.03 g  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE0.05 g  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE0.075 g  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE0.05 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
THEOBROMA CACAO WHOLE (UNII: EB048G1S9J)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)  
PROPYLENE GLYCOL PROPYL ETHER (UNII: 92KA3PYX0S)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
MEDIUM DENSITY POLYETHYLENE (UNII: 3W404QE89S)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 51239-3921-1100 in 1 CARTON12/01/202105/06/2025
17 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02012/01/202105/06/2025
Labeler - ITW Pro Brands (067952994)
Establishment
NameAddressID/FEIBusiness Operations
Lico Industries098009041manufacture(51239-3921)
Establishment
NameAddressID/FEIBusiness Operations
Prime Enterprises101946028manufacture(51239-3921) , analysis(51239-3921)

Revised: 10/2023
 

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