FDA.reportPublic FDA data

SCRUBS Sunscreen Lotion

Manufacturer
ITW Pro Brands | Lico Industries | Prime Enterprises
Effective date
2023-10-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:25:11

Label at a glance#

ProductScrubs Sunscren
Active ingredientAVOBENZONE, OCTOCRYLENE, HOMOSALATE, OCTISALATE
Label structure12 sections

Indications and uses

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

Dosage and administration

apply liberally 15 minutes before sun exposure reapply after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours

Storage and handling

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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Purpose

OTC - PURPOSE SECTION

Sunscreen

Sunscreen

Sunscreen

Sunscreen

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

OTC - ASK DOCTOR SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

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 INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

Uses & Directions Changes - effective 10-01-2022

RECENT MAJOR CHANGES SECTION

Uses:

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

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

Questions and comments?

OTC - QUESTIONS SECTION

Call: 1-877-684-5774

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SunscreenSunscreen

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51239-392151239-3921-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYSORBATE 207T1F30V5YHIACT
DISODIUM EDTA-COPPER6V475AX06UIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
METHYLCELLULOSE, UNSPECIFIEDZ944H5SN0HIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
THEOBROMA CACAO WHOLEEB048G1S9JIACT
WATER059QF0KO0RIACT
SODIUM HYDROXIDE55X04QC32IIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PEG-6 SORBITAN OLEATE58O7V09UCIIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
AVOBENZONEG63QQF2NOXACTIB
OCTOCRYLENE5A68WGF6WMACTIB
ACRYLATES CROSSPOLYMER-64GXD0Q3OS3IACT
PROPYLENE GLYCOL PROPYL ETHER92KA3PYX0SIACT
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
MEDIUM DENSITY POLYETHYLENE3W404QE89SIACT

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
06d645e3-1ac3-1031-e063-6394a90a0514d2425bd6-85db-2a64-e053-2995a90a2bd62023-10-03WarningsExact identifier
spl id: 06d645e3-1ac3-1031-e063-6394a90a0514
spl set id: d2425bd6-85db-2a64-e053-2995a90a2bd6

Reported adverse events (FAERS/openFDA)#

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