FDA.reportPublic FDA data

Clixit Airport Security Foot Wipes

Manufacturer
Renu Laboratories, Inc.
Effective date
2019-09-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:08:53

Label at a glance#

ProductClixit Airport Security Foot Wipes
Active ingredientTOLNAFTATE
Label structure10 sections

Indications and uses

Clinically proven to prevent most fungal nail and skin infections.

Dosage and administration

Wipe your feet including heels and between toes. For external use only

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

Clinically proven to prevent most fungal nail and skin infections.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Warnings

WARNINGS SECTION

  • Do not use on children under 2 years of age unless directed by a doctor
  • Avoid contact with eyes, ears or mouth
  • If irritation occurs, discontinue use and consult a doctor
  • If swallowed, get medical help or consult a poison control center immediately.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Ethoxydiglycol, Glycerin, Hippophae Rhamnoides (Sea Berry) Fruit and Seed Oil, Melaleuca Alternifolia (Tea Tree) Oil, Mentha Piperita (Peppermint) Leaf Oil, Menthol, Menthyl Lactate, PPG-20 Methyl Glucose Ether, Trimethylpentanediol/Adipic Acid Copolymer

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Wipe your feet including heels and between toes.

For external use only

STATEMENT OF IDENTITY SECTION

12 Single Use Individually Wrapped Towelettes

OUTSIDE CONTAINER

STATEMENT OF IDENTITY SECTION

12 pack BOX OF AIRPORT WIPES

Wipes_Box_12 COUNTWipes_Box_12 COUNT

single packette display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SINGLE AIRPORT PACKSINGLE AIRPORT PACK

SINGLE PACKETTE DISPLAY PANEL

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-44476348-444-01, 76348-444-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIETHYLENE GLYCOL MONOETHYL ETHERA1A1I8X02BIACT
GLYCERINPDC6A3C0OXIACT
TRIMETHYLPENTANEDIOL/ADIPIC ACID/GLYCERIN CROSSPOLYMER (25000 MPA.S)587WKM3S9QIACT
HIPPOPHAE RHAMNOIDES SEED OILT53SBG6741IACT
TOCOPHEROLR0ZB2556P8IACT
ALCOHOL3K9958V90MIACT
PEPPERMINT OILAV092KU4JHIACT
TEA TREE OILVIF565UC2GIACT
MENTHOLL7T10EIP3AIACT
HIPPOPHAE RHAMNOIDES FRUIT OILTA4JCF9S1JIACT
TOLNAFTATE06KB629TKVACTIB
MENTHYL LACTATE, (-)-2BF9E65L7IIACT
PPG-20 METHYL GLUCOSE ETHER3WV1T97D3KIACT

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
b8ba5c0e-e313-3a31-e053-2995a90a91e59353612b-cd48-0c25-e053-2a95a90af92e2021-01-12WarningsExact identifier
spl set id: 9353612b-cd48-0c25-e053-2a95a90af92e

Reported adverse events (FAERS/openFDA)#

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