SCRUBS SUNSCREN- 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]

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

Questions and comments?

Call: 1-877-684-5774

Package Label

INGREDIENTS AND APPEARANCE

SCRUBS SUNSCREN 
sunscreen lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51239-3921
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.03 g  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.05 g  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	0.075 g  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.05 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51239-3921-1	100 in 1 CARTON	12/01/2021	05/06/2025
1		7 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/01/2021	05/06/2025

Labeler - ITW Pro Brands (067952994)

Establishment
Name	Address	ID/FEI	Business Operations
Lico Industries		098009041	manufacture(51239-3921)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Enterprises		101946028	manufacture(51239-3921) , analysis(51239-3921)