WHITE RAIN FOAMING ANTIBACTERIAL HAND SPRING WATER- benzalkonium chloride liquid 
International Wholesale, Inc.

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White Rain Foaming Antibacterial Hand Soap Spring Water

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

External

for hand washing to decrease bacteria on the skin.

Warnings

for external use only.

When using this product 

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

Stop use and consult a doctor if:

irritation and redness develops.

Keep out of reach of children.

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

Directions:

Pump into DRY hands. Lather vigorously for at least 15 seconds. Rinse and dry thoroughly.

Inactive Ingredients

Water(Aqua), Lauramine Oxide, Cetrimonium Chloride, Myristamine Oxide, Glycerin, Coco-Glucoside, Glyceryl Oleate, Fragrance(Parfum), Citric Acid, Sodium Chloride, Disodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue No.1, FD&C Red 33.

Package Labeling:

Label

WHITE RAIN FOAMING ANTIBACTERIAL HAND SPRING WATER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52862-615
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
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
MYRISTAMINE OXIDE (UNII: J086PM3RRT)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
COCO GLUCOSIDE (UNII: ICS790225B)  
GLYCERYL OLEATE (UNII: 4PC054V79P)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52862-615-001 in 1 CASE01/01/2023
1177 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)01/01/2023
Labeler - International Wholesale, Inc. (161872676)

Revised: 11/2023
Document Id: 0a4d3bb3-2a76-06ab-e063-6394a90ac197
Set id: b695b136-24be-4ee1-8452-8c45f9dcafd1
Version: 4
Effective Time: 20231116
 
International Wholesale, Inc.