WHITE RAIN ANTIBACTERIAL HAND FRESH AND CLEAN- benzalkonium chloride soap

White Rain Antibacterial Hand Fresh and Clean by

Drug Labeling and Warnings

White Rain Antibacterial Hand Fresh and Clean 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

for hand washing, reduces germs on the skin

Warnings

for external use only-hands only.

Do Not use

on damaged or broken skin.

When using the product

keep out of eyes. Rinse with water to remove.

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:

Wash hands and rinse.

Inactive Ingredients

Water, Cetrimonium Chloride, Glycerin, Lauramidopropylamine Oxide and Myristamidopropylamine Oxide, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Citric Acid, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 5, Red 4

Other Information

Avoid storing at extreme temperatures.

Package Labeling:

INGREDIENTS AND APPEARANCE

WHITE RAIN ANTIBACTERIAL HAND FRESH AND CLEAN 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52862-627
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
TETRASODIUM EDTA (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52862-627-00	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/01/2025

Labeler - International Wholesale, Inc. (080442566)

Registrant - International Wholesale, Inc. (080442566)