FDA.reportPublic FDA data

Hypercln Sanitizing Wipes

Manufacturer
Falcon Safety Products, Inc. | Dan Mor
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:26:12

Label at a glance#

ProductHypercln Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

• Pull one sheet from container • Clean hands or affected area and discard • Close container after each use to keep wipes fresh

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride o.1%

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, except with adult supervision.

Warnings

WARNINGS SECTION

For external use only. Do not use in the eyes.

Keep out of eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult doctor if irritation persists for more than 72 hours.

If swallowed, seek medical attention or contact a Poison Control Center.

Use

DOSAGE & ADMINISTRATION SECTION

For use: gently pull wipe from the dispenser feed at an angle and in a downward motion. wet hands or surface thoroughly with the product and let dry, discard wipe in trash.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Fragrance, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate

Purpose

OTC - PURPOSE SECTION

Anti-bacterial

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate, Fragrance

Directions

INDICATIONS & USAGE SECTION

• Pull one sheet from container

• Clean hands or affected area and discard

• Close container after each use to keep wipes fresh

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hypercln 40Hypercln 40

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78847-22078847-220-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
WATER059QF0KO0RIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
SODIUM BENZOATEOJ245FE5EUIACT
EDETATE SODIUMMP1J8420LUIACT
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
SODIUM HYDROXYMETHYLGLYCINATEDIG6BWZ9XTIACT
CHAMOMILEFGL3685T2XIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PANTHENOLWV9CM0O67ZIACT

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
aa7c4c6f-9fd6-aab2-e053-2a95a90aca65a796b001-2d9b-89b1-e053-2995a90ac32c2020-07-15WarningsExact identifier
spl set id: a796b001-2d9b-89b1-e053-2995a90ac32c

Reported adverse events (FAERS/openFDA)#

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