NEOSPORIN LIP HEALTH OVERNIGHT RENEWAL THERAPY- petrolatum ointment

Neosporin Lip Health by

Drug Labeling and Warnings

Neosporin Lip Health by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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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)

INGREDIENTS AND APPEARANCE

NEOSPORIN LIP HEALTH   OVERNIGHT RENEWAL THERAPY
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0208
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Petrolatum (UNII: 4T6H12BN9U) (Petrolatum - UNII:4T6H12BN9U)	Petrolatum	774 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0208-1	1 in 1 BLISTER PACK	06/03/2009
1		7.7 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part347	06/03/2009

Labeler - Johnson & Johnson Consumer Inc. (002347102)