ANTIBACTERIAL CHERRY BLOSSOM- benzalkonium chloride soap

Antibacterial Cherry Blossom by

Drug Labeling and Warnings

Antibacterial Cherry Blossom 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, hexyl cinnamal, alpha-isomethyl ionone, disteareth-75 IPDI, PEG-150 distearate, citric acid, sodium chloride, tetrasodium EDTA, benzophenone-4, sodium benzoate, red 33

Adverse reation

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

FORMULA MADE IN USA

EMPLOYEE-OWNED

Prinsipal Display Panel

germ-x

ANTIBACTERIAL

LIQUID HAND SOAP

JASMINE & CHERRY BLOSSON SCENT

Dermatologist Tested

12FL OZ (355 ML)

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL CHERRY BLOSSOM 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-913
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)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
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)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-913-32	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(3)(a)	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(83986-913)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(83986-913)