NEOSPORIN LIP HEALTH  OVERNIGHT RENEWAL THERAPY- petrolatum ointment 
Johnson & Johnson Consumer 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

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

Other information

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 toll-free 800-223-0182 or 215-273-8755 (collect)

Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 7.7 g Jar Blister Pack

NEOSPORIN
LIP HEALTH ®

overnight renewal therapy ®
WHITE PETROLATUM LIP PROTECTANT
#1 DOCTOR RECOMMENDED BRAND™
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 TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0208
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM774 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LANOLIN (UNII: 7EV65EAW6H)  
PARAFFIN (UNII: I9O0E3H2ZE)  
COCOA BUTTER (UNII: 512OYT1CRR)  
MINERAL OIL (UNII: T5L8T28FGP)  
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIBEHENIN (UNII: 8OC9U7TQZ0)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
SODIUM PYRUVATE (UNII: POD38AIF08)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
CORN OIL (UNII: 8470G57WFM)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0208-11 in 1 BLISTER PACK06/03/2009
17.7 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34706/03/2009
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ee463053-5c9f-d84d-e053-2995a90a2aa9
Set id: 0da54fe1-c99f-4a2d-9ee5-2dc24005096c
Version: 5
Effective Time: 20230105
 
Johnson & Johnson Consumer Inc.