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Name:Neosporin Lip Health Overnight Renewal Therapy
Manufacturer:Johnson & Johnson Consumer Products Company, Division Of Johnson & Johnson Consumer Companies, Inc.
Category:Over-the-counter (OTC) Marketed Drugs


NEOSPORIN® Lip Health Overnight Renewal Therapy

NEOSPORIN LIP HEALTH  OVERNIGHT RENEWAL THERAPY - petrolatum ointment 
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, 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.

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NEOSPORIN® Lip Health Overnight Renewal Therapy

Drug Facts

Active ingredient

White petrolatum 77.4%

Purpose

Lip protectant

Uses

helps prevent and temporarily protects and helps relieve chapped or cracked lips

Warnings

For external use only

When using this product do not get into eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

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

Directions

apply as needed

Other information

  • store between 20° to 25 °C (68° - 77 °F)

Inactive ingredients

lanolin, paraffin, cocoa butter, mineral oil, flavor, VP/eicosene copolymer, ethylhexyl palmitate, titanium dioxide, tribehenin, vitamin E (dl-alpha tocopheryl acetate), sorbitan isostearate, sodium pyruvate, vitamin A palmitate, corn oil, cholecalciferol, palmitoyl oligopeptide

Questions?

call 1-800-223-0182

PRINCIPAL DISPLAY PANEL - 7.7 g Jar Blister Pack

NEOSPORIN®
LIP HEALTH™

overnight renewal therapy™
WHITE PETROLATUM LIP PROTECTANT

CLINICALLY
SHOWN TO:

Repair & nourish
as you sleep
Restore visibly
healthier lips in
3 NIGHTS

NET WT 0.27 oz (7.7g)

Principal Display Panel - 7.7 g Jar Blister Pack

NEOSPORIN LIP HEALTH   OVERNIGHT RENEWAL THERAPY
petrolatum ointment
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:58232-4035
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Petrolatum (Petrolatum) Petrolatum 774 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
Lanolin  
Paraffin  
Cocoa Butter  
Mineral Oil  
Ethylhexyl Palmitate  
Titanium Dioxide  
Tribehenin  
.Alpha.-Tocopherol Acetate, DL-  
Sodium Pyruvate  
Vitamin A Palmitate  
Corn Oil  
Cholecalciferol  
Palmitoyl Oligopeptide  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:58232-4035-1 1 JAR ( JAR) in 1 BLISTER PACK contains a JAR
1 7.7 g in 1 JAR This package is contained within the BLISTER PACK (58232-4035-1)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part347 06/03/2011

Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 06/2011 Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.



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


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