You are here: Home > Over-the-counter (OTC) Drugs > V > Virx (Ningbo Pulisi Daily Chemical Products Co., Ltd)

Name:Virx
Manufacturer:Ningbo Pulisi Daily Chemical Products Co., Ltd
Category:Over-the-counter (OTC) Marketed Drugs


Virx Instant Hand Sanitizer Drug Facts

VIRX  - alcohol gel 
Ningbo Pulisi Daily Chemical Products Co., Ltd

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.

----------

Virx Instant Hand Sanitizer Drug Facts

  • For external use only * Flammable * Keep away from fire or flame
  • Do not store above 40 degrees Celcius (105 degrees Fahrenheit)
  • Do not use in mouth, ears and eyes
  • When using this product, avoid contact with eyes
  • In case of contact, flush eyes with water

Deionized Water, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Aminomethyl Propanol, Carbomer, Fragrance. 

Ethyl Alcohol 62%......................................................................................Antiseptic

Keep out of reach of children. Children must be supervised when using this product.

Uses Hand Sanitizer to help decrease bacteria on the skin.

MM1


Bottle label

Stop use and seek a doctor if redness or irritation develops and persists for more than 72 hours.

Directions:
  • Pump as needed into your palms and thoroughly spread on both hands
  • Rub into skin until dry

VIRX 
instant hand sanitizer gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:40104-703
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Alcohol (Alcohol) Alcohol 618.1 mL  in 947 mL
Inactive Ingredients
Ingredient Name Strength
Water  
Glycerin  
Isopropyl Myristate  
Propylene Glycol  
ALPHA-TOCOPHEROL ACETATE  
Product Characteristics
Color yellow (yellow) Score     
Shape Size
Flavor LEMON (Lemon) Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:40104-703-22 947 mL in 1 BOTTLE, PUMP None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333 02/01/2010

Labeler - Ningbo Pulisi Daily Chemical Products Co., Ltd (529047265)
Registrant - Ningbo Pulisi Daily Chemical Products Co., Ltd (529047265)
Establishment
Name Address ID/FEI Operations
Ningbo Pulisi Daily Chemical Products Co., Ltd 529047265 manufacture

Revised: 02/2010 Ningbo Pulisi Daily Chemical Products Co., Ltd



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


Copyright © 2019 Drugsdb.eu by Dionisios Fentas || Terms of Use

Loading

OTC Marketed Drugs Alphabetically
A| B| C| D| E| F| G| H| I| J| K| L| M| N| O| P| Q| R| S| T| U| V| W| X| Y| Z| 0-9

Categories:
Prescription(RX) Drugs
Over-the-counter (OTC) Drugs
Homeopathic Drugs
Animal Drugs
Feedback