Hypercln Sanitizing Wipes

Hypercln Sanitizing Wipes by

Drug Labeling and Warnings

Hypercln Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Falcon Safety Products, Inc., Dan Mor. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HYPERCLN SANITIZING WIPES- anti-microbial cloth 
Falcon Safety Products, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hypercln Sanitizing Wipes

Directions

Directions for Use

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

Active Ingredient

Benzalkonium chloride 0.1%

Purpose

Anti-bacterial

Inactive Ingredients

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

Keep out of the reach of children.

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

Warnings

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.

To use

Wet hands or surface thoroughly with the product and let dry, discard wipe in trash.

Package Label

Hypercln 75

HYPERCLN SANITIZING WIPES 
anti-microbial cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78847-221
Route of AdministrationTRANSDERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.001 
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)  
PANTHENOL (UNII: WV9CM0O67Z)  
CHAMOMILE (UNII: FGL3685T2X)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
WATER (UNII: 059QF0KO0R)  
ALLANTOIN (UNII: 344S277G0Z)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
EDETATE SODIUM (UNII: MP1J8420LU)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78847-221-7575 in 1 POUCH; Type 0: Not a Combination Product06/12/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/12/202007/15/2020
Labeler - Falcon Safety Products, Inc. (150582500)
Registrant - Dan Mor (514523067)
Establishment
NameAddressID/FEIBusiness Operations
Dan Mor514523067manufacture(78847-221)

Revised: 7/2020
Document Id: aa7c5e04-3182-4477-e053-2995a90a66c9
Set id: a7e9ea97-2349-32a9-e053-2995a90adafa
Version: 2
Effective Time: 20200715