THE SPATHECARY FOAMING LAVENDER- benzalkonium chloride 0.13% soap 
Larry (Xiamen) Hi Tech Co., Ltd

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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The Spathecary Foaming Hand Soap Lavender

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

to help reduce bacteria that potentially can cause disease.

Warnings

For external use only.

When using this product

When using this product. Avoid contact with eyes. In case of eye contact, 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, get medical help or contact a Poison Control Center right away

Directions

Pump into hands, wet as needed. Lather vigorously for at least 20 seconds. Wash skin, rinse thoroughly, and dry.

Other Information

Store between 15-30C (59-86F)

Inactive Ingredients

aqua/water/EAU, Sodium Laureth Sulfate, cocamidopropylamine oxide, cocamidopropyl betaine, glycerin, parfum, methylchloroisothiazolinone, Methylisothiazolinone, Magnesium chloride, Magnesium nitrate, Aloe Barbadensis Leaf Juice, Disodium EDTA, Citric Acid, Tocopheryl Acetate, FD &C yellow No.5 (CI 19140), FD&C Red No. 33 (CI 17200), FD&C Blue No. 1 (CI 42090)

Questions or Comments?

P.O. Box 230258, Brooklyn, NY 11223

The Spathecary Foaming Hand Soap Lavender

label

THE SPATHECARY FOAMING LAVENDER 
benzalkonium chloride 0.13% soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73166-111
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.65 g  in 500 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73166-111-16500 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/01/2020
Labeler - Larry (Xiamen) Hi Tech Co., Ltd (529759328)
Registrant - G2 Beauty Inc (124608169)

Revised: 10/2020
Document Id: b1916fbe-58f5-41ab-e053-2995a90a86f4
Set id: b1916fbe-58f4-41ab-e053-2995a90a86f4
Version: 1
Effective Time: 20201013
 
Larry (Xiamen) Hi Tech Co., Ltd