Walgreens Citrus Antibacterial Foaming Hand: Package Insert and Label Information

WALGREENS CITRUS ANTIBACTERIAL FOAMING HAND- benzalkonium chloride soap
Walgreen Company

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.

Drug Facts

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, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamido-propylamine oxide, glycerin, fragrance, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, blue 1, red 33

Questions or comments?

1-800-925-4733

Company Information

DISTRIBUTED BY:

WALGREEN CO.

200 WILMOT RD.

DEERFIELD, IL 60015

Product Packaging

CITRUS

ANTIBACTERIAL

FOAMING

HAND SOAP

GENTLE & MILD

FORMULA

7.5 FL OZ (221 mL)

citrus hand soap
(click image for full-size original)
WALGREENS CITRUS ANTIBACTERIAL FOAMING HAND
benzalkonium chloride soap
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
LAURAMIDOPROPYLAMINE OXIDE
LAURAMINE OXIDE
CITRIC ACID MONOHYDRATE
SULISOBENZONE
COCAMIDOPROPYL BETAINE
MYRISTAMIDOPROPYLAMINE OXIDE
GLYCERIN
EDETATE SODIUM
SODIUM BENZOATE
FD&C BLUE NO. 1
D&C RED NO. 33
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-9002-01 221 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 08/10/2020
Labeler — Walgreen Company (008965063)

Revised: 08/2020 Walgreen Company

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