WHITE RAIN ANTIBACTERIAL HAND LEMON ZEST- benzalkonium chloride liquid

White Rain Antibacterial Hand Lemon Zest by

Drug Labeling and Warnings

White Rain Antibacterial Hand Lemon Zest 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, PEG-120 Methyl Glucose Dioleate, Myristamine Oxide, Cetrimonium Chloride, Glycerin, Coco-Glucoside, Glyceryl Oleate, Fragrance(Parfum), Citric Acid, Sodium Chloride, Disodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Yellow No.4, FD&C Red 33.

Package Labeling:

INGREDIENTS AND APPEARANCE

WHITE RAIN ANTIBACTERIAL HAND LEMON ZEST 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52862-616
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
WATER (UNII: 059QF0KO0R)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
MYRISTAMINE OXIDE (UNII: J086PM3RRT)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52862-616-00	1 in 1 CASE	01/01/2023
1		221 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)