FDA.reportPublic FDA data

KLENSKIN SUNBAR

Manufacturer
CoLabs Intl. Corp
Effective date
2016-03-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:27:53

Label at a glance#

ProductKLENSKIN SUNBAR SPF-20
Active ingredientAVOBENZONE, OCTOCRYLENE, OCTINOXATE
Label structure11 sections

Indications and uses

HELPS PREVENT SUNBURN IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS), DECREASES THE RISK OF SKIN CANCER AND EARLY SKIN AGING CAUSED BY THE SUN.

Dosage and administration

Apply liberally 15 minutes before sun exposure Reapply: • At least every 2 hours

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

OCTOCRYLENE 5.20%

OCTINOXATE 4.20%

AVOBENZONE 1.60%

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USES

INDICATIONS & USAGE SECTION

  • HELPS PREVENT SUNBURN
  • IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS), DECREASES THE RISK OF SKIN CANCER AND EARLY SKIN AGING CAUSED BY THE SUN.

WARNINGS

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY
  • DO NOT USE ON DAMAGED OR BROKEN SKIN.
  • WHEN USING THIS PRODUCT, KEEP OUT OF EYES AND RINSE WITH EXCESSIVE WATER TO REMOVE.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF PRODUCT IS SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

OTC - STOP USE SECTION

STOP USE AND ASK A DOCTOR IF RASH OR IRRITATION DEVELOPS.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure

  • Reapply: • At least every 2 hours

OTHER INFORMATION

OTHER SAFETY INFORMATION

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 of 15 or higher and other sun protection measures including:

Limit time in the sun, especially from 10a.m.-2p.m.
Wear long-sleeve shirts,pants, hats, and sunglasse
Childrenunder 6 months: Ask a doctor.


OTHER INFORMATION

  • PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUNLIGHT.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Sodium Stearate, Glycerin, Sodium Laureth Sulfate, Sorbitol, Sodium Lauryl Sulfate, Sodium Myristate, Sodium Cocoyl Isethionate, Acrylates Copolymer, Polyquaternium-16, Triethanolamine, Polyamide-3, Sorbitan Monooleate, Polysorbate 20,
Titanium Dioxide (opacifier), Carboxymethylcellulose Na, Polyethylene Glycol-16, Silica, Tetrasodium Etidronate, Pentasodium
Pentetate, DMDM Hydantoin Iodopropynyl Butylcarbamate, PG-Hydroxyethylcellulose, Stearyldimonium Chloride, Cocodimonium Hydroxypropyl Hydrolyzed Keratin

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

PLEASE CALL TOLL FREE 888.878.5536

WWW.KLENSKIN.COM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sunbar box finalsunbar box final

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61369-10461369-104-23

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OCTINOXATE4Y5P7MUD51ACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM STEARATEQU7E2XA9TGIACT
GLYCERINPDC6A3C0OXIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SORBITOL506T60A25RIACT
SODIUM LAURYL SULFATE368GB5141JIACT
SODIUM MYRISTATE06BLC4V0IVIACT
SODIUM COCOYL ISETHIONATE518XTE8493IACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
POLYQUATERNIUM-16 (N-VINYLPYRROLIDINONE:3-METHYL-1-VINYLIMIDAZOLIUM CHLORIDE (5:5))1KX12A42IJIACT
TROLAMINE9O3K93S3TKIACT
POLYACRYLAMIDE (1500 MW)5D6TC4BRWVIACT
SORBITAN MONOOLEATE06XEA2VD56IACT
POLYSORBATE 207T1F30V5YHIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
POLYETHYLENE GLYCOL 800UH6KR4953DIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
EDETATE SODIUMMP1J8420LUIACT
PENTASODIUM PENTETATE961TOZ5L7TIACT
DMDM HYDANTOINBYR0546TOWIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
PROPYLENE GLYCOL-HYDROXYETHYLCELLULOSE STEARYLDIMONIUM CHLORIDE3479326GXBIACT
HYDROLYZED WHEAT PROTEIN (ENZYMATIC; 3000 MW)J2S07SB0YLIACT

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
d0ea913f-2a12-40cb-91f9-623a0dfec154f1b2b228-b723-463d-ae9e-e5a970a6b7342019-12-04WarningsExact identifier
spl set id: f1b2b228-b723-463d-ae9e-e5a970a6b734

Reported adverse events (FAERS/openFDA)#

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