WHITE RAIN FOAMING ANTIBACTERIAL HAND SPRING WATER- benzalkonium chloride liquid

White Rain Foaming Antibacterial Hand Spring Water by

Drug Labeling and Warnings

White Rain Foaming Antibacterial Hand Spring Water by is a Otc medication manufactured, distributed, or labeled by International Wholesale, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

INGREDIENTS AND APPEARANCE

WHITE RAIN FOAMING ANTIBACTERIAL HAND SPRING WATER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52862-615
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52862-615-00	1 in 1 CASE	01/01/2023
1		177 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2023

Labeler - International Wholesale, Inc. (161872676)