ANTIBACTERIAL HAND WHITE TEA AND EUCALYPTUS- benzalkonium chloride soap

Antibacterial Hand White Tea and Eucalyptus by

Drug Labeling and Warnings

Antibacterial Hand White Tea and Eucalyptus by is a Otc medication manufactured, distributed, or labeled by UpLift Brands LLC, Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

• avoid contact with eyes. If contact occurs, rinse eyes with water.

Stop use and ask a doctor if 

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

• wet hands 
• apply palmful to hands 
• scrub thoroughly 
• rinse thoroughly

Inactive Ingredients 

water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, glycerin, myristamidopropylamine oxide, fragrance, linalool, disteareth-75 IPDI, PEG-150 distearate, citric acid, sodium chloride, tetrasodium EDTA, benzophenone-4, sodium benzoate, ext. violet 2

Adverse reaction

Distributed by: Vi-Jon, LLC, St. Louis, MO 63114

FORMULA MADE IN USA

EMPLOYEE-OWNED

Principal Panel Display

germ-x

ANTIBACTERIAL

LIQUID HAND SOAP

WHITE TEA & EUCALYPTUS SCENT

Dermatologist Tested

12 FL OZ (355 mL)

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND WHITE TEA AND EUCALYPTUS 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-140
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)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
GLYCERIN (UNII: PDC6A3C0OX)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE SODIUM (UNII: MP1J8420LU)
SULISOBENZONE (UNII: 1W6L629B4K)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-140-32	355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/12/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/12/2022

Labeler - UpLift Brands LLC (119091527)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(83986-140)