Beard Society American Edition Antibacterial Hand Soap

Beard Society American Edition Antibacterial Hand by

Drug Labeling and Warnings

Beard Society American Edition Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Kira Labs Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BEARD SOCIETY AMERICAN EDITION ANTIBACTERIAL HAND- benzalkonium chloride gel 
Kira Labs 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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Beard Society American Edition Antibacterial Hand Soap

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use(s)

Helps eliminate bacteria on skin

Warnings

For external use only.

When using this product

avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor

if irritation or rash appears and lasts for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Pump onto wet hands. Work into a rich lather and scrub hands for 20 seconds or more to fight germs. Rinse clean and repeat as needed.

 Children under 6 years should be supervised when using this product.

Inactive ingredients

Purified Water, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Cocamide MEA, Cocamidopropyl Betaine, Sodium Chloride, Fragrance, Propylene Glycol, Methylchloroisothiazolinone, Methylisothiazolinone, Disodium EDTA, Tocopherol, Glycerin, Aloe Barbadensis Leaf Juice, Citric Acid

Package Labeling:

Bottle

BEARD SOCIETY AMERICAN EDITION ANTIBACTERIAL HAND 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 77816-515
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
TOCOPHEROL (UNII: R0ZB2556P8)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 77816-515-01480 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/202010/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/01/202010/31/2022
Labeler - Kira Labs Inc (132579397)

Revised: 7/2021
 

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