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

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White Rain Antibacterial Hand Soap SPRING WATER

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

for hand washing to decrease bacteria on the skin. External

Warnings

for external use only.   

When using this product

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

Stop 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, Coco-Glucoside, Glyceryl Oleate, Cetrimonium Chloride, PEG-150 Distearate, Myristamine Oxide, Glycerin, Fragrance(Parfum), Citric Acid, Sodium Chloride, Disodium EDTA, Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Red 33, FD&C Blue No. 1.

Package Labeling:

Label5

WHITE RAIN ANTIBACTERIAL HAND SPRING WATER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52862-624
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)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
COCO GLUCOSIDE (UNII: ICS790225B)  
GLYCERYL OLEATE (UNII: 4PC054V79P)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
MYRISTAMINE OXIDE (UNII: J086PM3RRT)  
GLYCERIN (UNII: PDC6A3C0OX)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
SULISOBENZONE (UNII: 1W6L629B4K)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52862-624-001 in 1 CASE02/01/2023
1221 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)02/01/2023
Labeler - International Wholesale, Inc. (161872676)

Revised: 11/2023
Document Id: 0a4d3265-080d-d2ed-e063-6394a90adbee
Set id: e64dbfa2-6f04-4d67-b066-47dd24bc4dfb
Version: 3
Effective Time: 20231116
 
International Wholesale, Inc.