MOISTURIZING ANTIBACTERIAL- benzalkonium chloride 0.13% soap

Moisturizing Antibacterial by

Drug Labeling and Warnings

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

Drug Details [pdf]

Inactive 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, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, Citrus nobilis (mandarin orange) oil, Camellia sinensis leaf extract, Zingiber officinale (ginger) root oil, blue 1, yellow 5

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by Colgate-Palmolive Company, distributor of Softsoap Antibacterial Liquid Hand Soap Fresh Citrus

DISTRIBUTED BY

MEIJER DISTRIBUTION, INC.,

GRAND RAPIDS, MI 49544

www.meijer.com

how2recycle.info

Empty & Discard Pump

Plastic Bottle

principal display panel

Meijer

Compare to Softsoap*

Antibacterial Hand Soap

Fresh Citrus

Paraben Free

11.25 FL OZ (332 mL)

INGREDIENTS AND APPEARANCE

MOISTURIZING ANTIBACTERIAL 
benzalkonium chloride 0.13% soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79481-9633
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)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
GLYCERIN (UNII: PDC6A3C0OX)
DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
SULISOBENZONE (UNII: 1W6L629B4K)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ORANGE OIL (UNII: AKN3KSD11B)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
GINGER OIL (UNII: SAS9Z1SVUK)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79481-9633-1	332 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/26/2016
2	NDC: 79481-9633-2	1650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/26/2016	07/05/2020
3	NDC: 79481-9633-3	1479 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/26/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/26/2016

Labeler - MEIJER (006959555)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(79481-9633)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(79481-9633)