SCRUBS SUNSCREEN- sunscreen lotion

Scrubs Sunscreen by

Drug Labeling and Warnings

Scrubs Sunscreen by is a Otc medication manufactured, distributed, or labeled by ITW Pro Brands, CoreTex Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Avobenzone 1.0%..........Sunscreen

Homosalate 5.0%...........Sunscreen
Octinoxate 7.5%.............Sunscreen
Octisalate 5.0%..............Sunscreen
Oxybenzone 6.0%..........Sunscreen

USAGE

-Helps prevent sunburn

-If used as directed with other sun measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNING

For external use only

Do not use on damaged or broken skin.

When using the product, keep out of eyes, rinse with water to remove.

DIRECTIONS

Directions

-apply liberally (or generously) and evenly 15 minutes before sun exposure.

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 Value of 15 or higher and other sun protection measures including:

-limit time in the sum, especially from 10 a.m. – 2 p.m.

-wear long-sleeved shirts, pants, hats, and sunglasses

reapply:

-after 80 minutes of swimming or sweating.

-immmediatly after towel drying.

-at least every 2 hours.

Children under 6 months of age: Ask a doctor.

INACTIVE INGREDIENTS

Acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis (aloe vera) leaf juice, butylparaben, carbomer, calendula officinalis flower extract, chamomile recutita (matricaria) extract, C12-15 alkyl benzoate, dimethicone, dimethyl capramide, ethylparaben, fragrance (parfum), glyceryl stearate, isobutylparaben, methylparaben, nasturtium officinale (watercress) extract, peg-100 stearate, phenoxyethanol, propylparaben, symphytum officinale (comfrey) leaf extract, tetrasodium EDTA, tocopherol, tocopheryl acetate, triethanolamine, water.

STORAGE AND HANDLING

Protect this product from excessive heat and sun.

ASK A DOCTOR

Stop use and ask a doctor if a rash occurs.

KEEP OUT OF THE REACH OF CHILDREN

Keep out of the reach of children

if swallowed get medical help or contact a Poison Control Center right away.

PURPOSE

Sunscreen

PACKAGE LABEL

INGREDIENTS AND APPEARANCE

SCRUBS SUNSCREEN 
sunscreen lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51239-2921
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.05 g  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	0.06 g  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	0.05 g  in 1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.075 g  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.01 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)
SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
DIMETHICONE 200 (UNII: RGS4T2AS00)
PEG-100 STEARATE (UNII: YD01N1999R)
TOCOPHEROL (UNII: R0ZB2556P8)
C12-20 ALKYL BENZOATE (UNII: Y15I6XI14C)
ETHYLPARABEN (UNII: 14255EXE39)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATERCRESS (UNII: K5877MW0LE)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CHAMOMILE (UNII: FGL3685T2X)
DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51239-2921-0	7 g in 1 POUCH; Type 0: Not a Combination Product	05/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	05/01/2017

Labeler - ITW Pro Brands (067952994)

Establishment
Name	Address	ID/FEI	Business Operations
Pure Source, LLC		080354456	manufacture(51239-2921) , analysis(51239-2921)

Establishment
Name	Address	ID/FEI	Business Operations
Lico Industries		098009041	pack(51239-2921) , label(51239-2921)