OTC Medication Information: Moisturizing Hand Sanitizer

MOISTURIZING HAND SANITIZER- alcohol lotion
Vi-Jon, LLC

Claims

germ-x

MOISTURIZING

FOAMING

HAND SANITIZER

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For external use only: hands only

Flammable, keep away from fire or flame.

When using this product

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

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 thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Inactive ingredients

water, PEG-8 dimethicone, meadowfoamamidopropyl betaine, glycerin, tocopheryl acetate, isopropyl myristate

Adverse Reactions Section

Distributed By: Vi-Jon, LLC

St. Louis, MO 63114

Principal display panel

germ-X®

MOISTURIZING

FOAMING

HAND SANITIZER

1150 mL (39 FL OZ)

image description
(click image for full-size original)
MOISTURIZING HAND SANITIZER
ethyl alcohol lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11344-447
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Alcohol (ALCOHOL) Alcohol .62 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
water
PEG-8 DIMETHICONE
MEADOWFOAMAMIDOPROPYL BETAINE
GLYCERIN
.ALPHA.-TOCOPHEROL ACETATE
ISOPROPYL MYRISTATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:11344-447-08 1150 mL in 1 BOTTLE, PLASTIC None
2 NDC:11344-447-04 750 mL in 1 BOTTLE, PLASTIC None
3 NDC:11344-447-45 1150 mL in 1 BOTTLE, PLASTIC None
4 NDC:11344-447-44 532 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M505(a)(3) 05/03/2016
Labeler — Vi-Jon, LLC (088520668)
Registrant — Vi-Jon, LLC (790752542)
Establishment
Name Address ID/FEI Operations
Vi-Jon, LLC 088520668 manufacture (11344-447)
Establishment
Name Address ID/FEI Operations
Vi-Jon, LLC 790752542 manufacture (11344-447)

Revised: 11/2023 Vi-Jon, LLC

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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