ANTIBACTERIAL BODY WASH- benzalkonium chloride lotion
UNFI

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Equaline 337.002/337AB Antibacterial Body Wash

Active ingredients

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

to decrease bacteria on the skin

Warnings

For external use only

When using this product

do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Keep out of reach of children

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

Directions

work a small amount into a lather
scrub thoroughly
rinse

inactive ingredients

water, PEG-120 methyl glucose dioleate, cetrimonium chloride, glycerin, lauramidopropylamine oxide, cocamide MEA, fragrance, sodium sulfate, myristamidopropylamine oxide, sodioum chloride, citric acid, tetrasodium EDTA, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33

EQUALINE

Antbacterial Body Wash

Spring Fresh

EQUALINE - for shoppers who know qualty doesn't always mean expensive

Enjoy the tantalizing fragrance of our moisturizing, antibacterial formula that will caress your skin and leave it clean and soft.

DISTRIBUTED BY SUPERVALU INC

EDEN PRAIRIE,MN 55344

We're committed to your satisfaction and guarantee the quality of this product. Contact us at 1-877-932-7948, or www.supervalu-ourownbrands.com.

Please have package ready.

principal display panel

EQUALINE

Antibacterial Body Wash

Spring Fresh

Antibacterial cleanser plus moistuizer

21 FL OZ (621 mL)

image description

ANTIBACTERIAL BODY WASH
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41163-898
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.313 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
water (UNII: 059QF0KO0R)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
cetrimonium chloride (UNII: UC9PE95IBP)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
SODIUM SULFATE (UNII: 0YPR65R21J)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
methylchloroisothiazolinone (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:41163-898-56	621 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/08/2015	10/07/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/08/2015	10/07/2021

Labeler - UNFI (006961411)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		088520668	manufacture(41163-898)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		790752542	manufacture(41163-898)

Revised: 10/2021

Document Id: 8f73a629-fae3-40b8-9b98-faa093042a5d

Set id: de301897-1ca0-478b-9149-64c98ca97ea9

Version: 8

Effective Time: 20211007

UNFI