FDA.reportPublic FDA data

Laura Lynn Antibacterial Liquid Hand Soap

Manufacturer
Ingles Markets, Inc.
Effective date
2026-07-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-04 03:33:26

Label at a glance#

ProductLaura Lynn Antibacterial Liquid Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Pump onto dry hands. Lather vigorously for at least 15 seconds. Rinse and dry thoroughly.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For hand washing to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Do not use on children less than 2 months of age or on open skin wounds.

When using this product avoid contact with eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs.

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

  • Pump onto dry hands.
  • Lather vigorously for at least 15 seconds.
  • Rinse and dry thoroughly.

Other Information

OTHER SAFETY INFORMATION

  • Store between 59-86 ºF (15-30 ºC)
  • Avoid freezing and excessive heat above 104 ºF (40 ºC)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Sodium Chloride, Sodium Lauryl Sulfate, Cocamidopropyl Betaine, Glycerin, Fragrance, Tocopheryl Acetate, Methylchloroisothiazolinone, Methylisothiazolinone, Aloe Barbadensis Leaf Juice, Yellow 5, Red 4

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label - 8 fl. oz. Bottle with Pump_FrontProduct Label - 8 fl. oz. Bottle with Pump_Front

Product Label - 8 fl. oz. Bottle with Pump_Front (2041)

Product Label - 8 fl. oz. Bottle with Pump_BackProduct Label - 8 fl. oz. Bottle with Pump_Back

Product Label - 8 fl. oz. Bottle with Pump_Back (2042)

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130086854074275GTIN-13: 0086854074275
EAN-13: 0086854074275
GTIN-12: 086854074275
UPC-A: 086854074275
GTIN storage (14 digits): 00086854074275		LLALHS_08Back.jpg

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62936-015062936-0150-6, 62936-0150-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM LAURYL SULFATE368GB5141JIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE15O9QS218WIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C RED NO. 4X3W0AM1JLXIACT

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
Laura Lynn Antibacterial Liquid HandBENZALKONIUM CHLORIDEIngles Markets, Inc.57ed13d7-0f68-ae4f-e063-6294a90ab7d22026-07-01WarningsExact identifier
ndc (package): 62936-0150-3
ndc (package): 62936-0150-6
ndc (product): 62936-0150
ndc11 (package): 62936015003
ndc11 (package): 62936015006
spl id: 57ed11c8-9970-9585-e063-6394a90a2483
spl set id: 57ed13d7-0f68-ae4f-e063-6294a90ab7d2

Reported adverse events (FAERS/openFDA)#

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