Laura Lynn Antibacterial Liquid Hand Soap

Laura Lynn Antibacterial Liquid by

Drug Labeling and Warnings

Laura Lynn Antibacterial Liquid by is a Otc medication manufactured, distributed, or labeled by Dyno Manufacturing. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

LAURA LYNN ANTIBACTERIAL LIQUID 
benzalkonium chloride 0.13% soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79532-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.306 g  in 236 mL

Inactive Ingredients
Ingredient Name	Strength
.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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79532-023-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2023
2	NDC: 79532-023-53	1570 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/01/2023

Labeler - Dyno Manufacturing (015718256)

Revised: 8/2023

Document Id: 04265230-e633-c9aa-e063-6394a90a9b32

34390-5

Set id: 04269f25-ab80-27a7-e063-6394a90abaec

Version: 1

Effective Time: 20230830