FDA.reportPublic FDA data

Hypercln

Manufacturer
Falcon Safety Products, Inc. | Dan Mor
Effective date
2020-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:25:49

Label at a glance#

ProductHypercln
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

1. Tear open and unfold wipe 2. Sanitize hands and affected area. 3. Discard in trash after use. Do not flush.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Anti-bacterial

Keep out of the 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.

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

DOSAGE & ADMINISTRATION SECTION

1. Tear open and unfold wipe 2. Sanitize hands and affected area. 3. Discard in trash after use. Do not flush.

Use

INDICATIONS & USAGE SECTION

1. Tear open and unfold wipe. 2. Sanitize hands and affected area. 3. Discard in trash after use. Do not flush.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HyperclnHypercln

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78847-22278847-222-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
CHAMOMILEFGL3685T2XIACT
EDETATE SODIUMMP1J8420LUIACT
ALLANTOIN344S277G0ZIACT
PANTHENOLWV9CM0O67ZIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
SODIUM HYDROXYMETHYLGLYCINATEDIG6BWZ9XTIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT

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
aa7c5e04-3180-4477-e053-2995a90a66c9a7eb256c-24ef-20e7-e053-2a95a90aecfa2020-07-15WarningsExact identifier
spl set id: a7eb256c-24ef-20e7-e053-2a95a90aecfa

Reported adverse events (FAERS/openFDA)#

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