SCRUBS Sunscreen Lotion

Manufacturer
ITW Pro Brands | Pure Source, LLC | Lico Industries
Effective date
2021-12-03
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 22:24:51

Label at a glance#

ProductScrubs Sunscreen
Active ingredientOCTISALATE, OXYBENZONE, HOMOSALATE, OCTINOXATE, AVOBENZONE
Label structure10 sections

Dosage and administration

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 shi...

Storage and handling

Protect this product from excessive heat and sun.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Purpose

0.070g Avobenzone 1.0%..........Sunscreen
0.350g Homosalate 5.0%...........Sunscreen
0.525g Octinoxate 7.5%.............Sunscreen
0.350g Octisalate 5.0%..............Sunscreen
0.420g Oxybenzone 6.0%..........Sunscreen

USAGE

INDICATIONS & USAGE SECTION

-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

WARNINGS SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and sun.

ASK A DOCTOR

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if a rash occurs.

KEEP OUT OF THE REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

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

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SCRUB SunscreenSCRUB Sunscreen

Products#

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DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51239-192151239-1921-0

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d24263cc-d418-61fb-e053-2995a90a4e227b6b75a5-d433-5a5c-e053-2a91aa0a4d8d2021-12-03WarningsExact identifier
spl id: d24263cc-d418-61fb-e053-2995a90a4e22
spl set id: 7b6b75a5-d433-5a5c-e053-2a91aa0a4d8d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.