FDA.reportPublic FDA data

Laflare Santix Antibacterial Moisturizing Wipes

Manufacturer
NAICO
Effective date
2020-05-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:28:19

Label at a glance#

ProductLaflare Santix Antibacterial Moisturizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

Instant hand antimicrobial to decrease bacteria on the skin

Dosage and administration

■ Wet hands thoroughly with product and allow to dry without wiping ■ Do not flush

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Glycerin, Sodium Benzoate, Polysorbate 20, Disodium EDTA, Citric Acid, Tocopheryl Acetate, Macadamia Integrifolia/Tetraphylla Seed Oil, Anthemis Nobilis Flower Extract, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Antimicrobial

WARNINGS

WARNINGS SECTION

For external use only.
--------------------------------------------------------------------------------------------------------
Do not use
• in children less than 2 months of age
• on open skin wounds
--------------------------------------------------------------------------------------------------------
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Posion Control Center right away

Uses

INDICATIONS & USAGE SECTION

Instant hand antimicrobial to decrease bacteria on the skin

Directions

DOSAGE & ADMINISTRATION SECTION

■ Wet hands thoroughly with product and allow to dry without wiping

■ Do not flush

Other information

OTHER SAFETY INFORMATION

Storage in a cool, dry place, Avoid freezing and excessive heat above 40 ℃ (104 ℉)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of containerImage of container

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75536-0005-12025-01-06C16284748780-1d6a99b39-3ed4-a426-e053-dadaa90af4c2Drug Facts
75536-0005-12022-01-28C16284748780-1d6a99b39-3ed4-a426-e053-dadaa90af4c2Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75536-000575536-0005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
SODIUM BENZOATEOJ245FE5EUIACT
Polysorbate 207T1F30V5YHIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CHAMAEMELUM NOBILE FLOWERO2T154T6OGIACT

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
2b055781-75c6-a401-e063-6394a90a0a4c7b6f8f2f-c020-4ba6-85cb-d1f55f1169f92025-01-06WarningsExact identifier
spl set id: 7b6f8f2f-c020-4ba6-85cb-d1f55f1169f9

Reported adverse events (FAERS/openFDA)#

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