OTC Medication Information: Premium Hand Sanitizer

PREMIUM HAND SANITIZER- alcohol gel
MCKESSON MEDICAL-SURGICAL 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.

Active Ingredient Purpose

Ethanol 70% ……………………………….. hand sanitizer

Uses

  • an antiseptic hand sanitizer for topical application
  • helps prevent infection and cross-contamination
  • reduces transient microorganisms on intact skin
  • recommended for repeated use

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

McKesson Premium Hand Sanitizer

With Vitamin E, Moisturizers, & Emollients

For frequent use

Directions

Wet hands thoroughly with product. Allow to dry without wiping. Use no water or towels.

Warnings

For external use only.

Flammable, keep away from fire or flame.

When using this product  avoid contact with eyes. In case of eye contact, flush with water for 15 minutes.

Discontinue use and see a doctor if  irritation occurs.

Avoid contact with broken skin.

Inactive ingredients

purified water, carbomer, glycerin, isopropyl myristate, tocopherol (vitamin E), diisopropyl sebacate, isopropanol, propylene glycol, aminomethyl propanol, fragrance, blue 1.

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PREMIUM HAND SANITIZER
ethanol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:68599-5201
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 70 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
CARBOMER COPOLYMER TYPE A
GLYCERIN
ISOPROPYL MYRISTATE
TOCOPHEROL
DIISOPROPYL SEBACATE
ISOPROPYL ALCOHOL
PROPYLENE GLYCOL
AMINOMETHYLPROPANOL
FD&C BLUE NO. 1
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68599-5201-1 118 g in 1 PACKAGE None
2 NDC:68599-5201-2 237 g in 1 PACKAGE None
3 NDC:68599-5201-3 532 g in 1 PACKAGE None
4 NDC:68599-5201-4 1000 g in 1 PACKAGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/09/2015
Labeler — MCKESSON MEDICAL-SURGICAL INC. (023904428)

Revised: 11/2019 MCKESSON MEDICAL-SURGICAL 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.

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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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