OTC Medication Information: Antibacterial Hand Wash

ANTIBACTERIAL HAND WASH- benzalkonium chloride liquid
Intercon Chemical Co.

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

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

  • avoid contact with the eyes. If contact occurs, rinse eyes 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, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, fragrance, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, red 4, yellow 5

ClearlyBetter

by INTERCON

ANTIBACTERIAL FOAMING HAND SOAP

DISTRIBUTED BY: INTERCON CHEMICAL CO.

1100 CENTRAL INDUSTRIAL DR.

ST. LOUIS, MO 63110

principal display panel

ClearlyBetter

BY INTERCON

ANTIBACTERIAL FOAMING HAND SOAP

1150 mL (39 FL OZ)

image description
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ANTIBACTERIAL HAND WASH
benzalkonium chloride 0.13% liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:67502-460
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.313 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
water
COCAMIDOPROPYL BETAINE
LAURAMIDOPROPYLAMINE OXIDE
LAURAMINE OXIDE
MYRISTAMIDOPROPYLAMINE OXIDE
GLYCERIN
CITRIC ACID MONOHYDRATE
EDETATE SODIUM
SULISOBENZONE
SODIUM BENZOATE
FD&C RED NO. 4
FD&C YELLOW NO. 5
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:67502-460-27 1150 mL in 1 BOTTLE, PLASTIC None
2 NDC:67502-460-07 750 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 09/08/2016
Labeler — Intercon Chemical Co. (103204970)
Registrant — Vi-Jon, LLC (790752542)
Establishment
Name Address ID/FEI Operations
Vi-Jon. LLC 150931459 manufacture (67502-460)

Revised: 06/2021 Intercon Chemical Co.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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