OTC Medication Information: Jergens Moisture Care Hand Sanitizer

JERGENS MOISTURE CARE HAND SANITIZER- benzalkonium chloride cream
Kao USA Inc.

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

Antiseptic

Use

  • hand sanitizer to help reduce bacteria on the skin
  • recommended for repeated use

Warnings

For external use only

When using this product avoid contact with eyes. If contact occurs rinse thoroughly with water.

Stop use and ask a doctor if

  • irritation or redness develops.
  • conditions persist 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 thoroughly with product and allow to dry without wiping
  • children under 6 years of age should be supervised when using this product
  • not recommended for infants

Other information store at room temperature

Inactive ingredients water, glycerin, petrolatum, cetearyl alcohol, isopropyl palmitate, behentremonium chloride, paraffin, stearyl alcohol, dimethicone, aluminum starch octenylsuccinate, isopropyl alcohol, fragrance, alcohol, cetyl-PG hydroxyethyl palmitamide, cocos nucifera (coconut) oil, tocopheryl acetate, butylene glycol, eucalyptus globulus leaf extract, methylparaben, ethylparaben

* kills 99.9% of common harmful germs such as bacteria

Questions or comments? Jergens Skincare Experts are always at your fingertips: www.jergens.com or call 1-800-742-8798

JERGENS is a trademark of Kao Corp.

Distributed by Kao USA Inc., Cincinnati, OH 45214 ©2020

Made in USA of US & Imported Ingredients

JERGENS

MOISTURE CARE

Hand Sanitizer Cream

KILLS 99.9% OF GERMS*

Vitamin E & Coconut Oil NOURISHES DRY HANDS

7.5 FL OZ (221 mL)

10596-717 Hand Sanitizer
(click image for full-size original)
JERGENS MOISTURE CARE HAND SANITIZER
benzalkonium chloride cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:10596-717
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.13 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
BEHENTRIMONIUM CHLORIDE
ALCOHOL
HYDROXYETHYL PALMITYL OXYHYDROXYPROPYL PALMITAMIDE
ALPHA-TOCOPHEROL ACETATE
COCONUT OIL
BUTYLENE GLYCOL
EUCALYPTUS GLOBULUS LEAF
METHYLPARABEN
ETHYLPARABEN
WATER
GLYCERIN
CETOSTEARYL ALCOHOL
PETROLATUM
ISOPROPYL PALMITATE
PARAFFIN
STEARYL ALCOHOL
DIMETHICONE
ALUMINUM STARCH OCTENYLSUCCINATE
ISOPROPYL ALCOHOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:10596-717-30 88 mL in 1 TUBE None
2 NDC:10596-717-75 221 mL in 1 TUBE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 01/01/2021
Labeler — Kao USA Inc. (004251617)

Revised: 10/2020 Kao USA Inc.

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.

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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