Walgreens ANTIBACTERIAL HAND REFILL: Package Insert and Label Information

WALGREENS ANTIBACTERIAL HAND REFILL- benzalkonium chloride liquid
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.

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

Helps eliminate bacteria on hands

Warnings

For external use only.

When using this product

avoid contact with eyes. In case of contact, rinse thoroughly with water.

Stop use and ask doctor if

irritation or redness develops and lasts.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

  • use to refill a hand soap pump bottle
  • from pump bottle, apply onto wet hands
  • lather and rinse thoroughly

Other informaton

store at room temperature

Inactive ingredients

Water (Aqua), Lauramidopropylamine Oxide, Glycerin, Cetrimonium Chloride, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Sulfate, Methylchloroisothiazolinone, Methylisothiazolinone, Red 40 (CI 16035), Yellow 5 (CI 19140), Red 33 (CI 17200)

Questions or comments?

1-800-925-4733

Label Copy

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WALGREENS ANTIBACTERIAL HAND REFILL
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7211
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
CETRIMONIUM CHLORIDE
GLYCERIN
LAURAMIDOPROPYLAMINE OXIDE
COCO MONOETHANOLAMIDE
SODIUM CHLORIDE
PEG-120 METHYL GLUCOSE DIOLEATE
CITRIC ACID MONOHYDRATE
EDETATE SODIUM
SODIUM SULFATE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C RED NO. 40
FD&C YELLOW NO. 5
D&C RED NO. 33
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-7211-56 1650 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 part333E 04/22/2019
Labeler — WALGREEN COMPANY (008965063)
Registrant — APOLLO HEALTH AND BEAUTY CARE INC. (201901209)
Establishment
Name Address ID/FEI Operations
APOLLO HEALTH AND BEAUTY CARE INC. 201901209 manufacture (0363-7211)

Revised: 09/2022 WALGREEN COMPANY

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