LAURA LYNN ANTIBACTERIAL LIQUID- benzalkonium chloride 0.13% soap 
Dyno Manufacturing

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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Laura Lynn Antibacterial Liquid Hand Soap

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

For hand washing to help reduce bacteria on the skin

Warnings

For external use only.

Do Not Use

  • In children less that 2 months of age
  • on open skin wounds

When using this product

Avoid contact with eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

  • Pump onto dry hand
  • Lather vigorously for at least 15 seconds.
  • Rinse and dry thoroughly

Other Information

Store between 15-30C (59-86F)
Avoid Freezing and excessive heat above 40C (104F)

Inactive Ingredients

Water, Sodium Lauryl Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Glycerin, Aloe Barbadensis, Fragrance,Sodium Laureth Sulfate, Methylchloroisothiazolinone, Methylisothiazolinone,Tocopherol Acetate, Yellow 5, Red 4

Laura Lynn Antibacterial Liquid Hand Soap

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LAURA LYNN ANTIBACTERIAL LIQUID 
benzalkonium chloride 0.13% soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79532-023
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.306 g  in 236 mL
Inactive Ingredients
Ingredient NameStrength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79532-023-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2023
2NDC:79532-023-531570 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/01/2023
Labeler - Dyno Manufacturing (015718256)

Revised: 8/2023
Document Id: 04265230-e633-c9aa-e063-6394a90a9b32
Set id: 04269f25-ab80-27a7-e063-6394a90abaec
Version: 1
Effective Time: 20230830
 
Dyno Manufacturing