Germ-X 818.001/818AA rev 1

Moisturizing Antibacterial by

Drug Labeling and Warnings

Moisturizing Antibacterial by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MOISTURIZING ANTIBACTERIAL- benzalkonium chloride 0.13% soap 
Consumer Product Partners, LLC

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Germ-X 818.001/818AA rev 1

claims

ANTIBACTERIAL HAND SOAP

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 thoroughly with water

Stop use and ask a doctor if

• irritation or redness develops
• 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, sodium chloride
myristamidopropylamine oxide, glycerin, fragrance, hexyl cinnamal, linalool, benzyl salicylate, butylphenyl methylpropional, Aloe barbadensis leaf juice, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, yellow 10, green 3

disclaimer

*Washing hands helps wash away bacteria and germs

Adverse Reactions

Dist. by: Vi-Jon, LLC.,

8515 Page Ave, St. Louis, MO 63114

principal display panel

germ-X ,

ANTIBACTERIAL

HAND SOAP WITH ALOE

WASHES AWAY GERMS*

pH Balanced

Dermatologist Tested

FORMULA MADE IN USA

EMPLOYEE-OWNED

12 FL OZ (354 mL)

MOISTURIZING ANTIBACTERIAL 
benzalkonium chloride 0.13% soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-818
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 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
SULISOBENZONE (UNII: 1W6L629B4K)
SODIUM BENZOATE (UNII: OJ245FE5EU)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-818-32	354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/05/2022	09/03/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/05/2022	09/03/2022

Labeler - Consumer Product Partners, LLC (119091520)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, LLC		790752542	manufacture(11344-818)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, LLC		088520668	manufacture(11344-818)

Revised: 2/2024

Document Id: 10d1ce4a-229d-31e2-e063-6294a90a4391

34390-5

Set id: 03bb52e3-cddc-481e-bd92-4923da631f7c

Version: 18

Effective Time: 20240207